Inbentus Versatile
Device Facts
| Record ID | K252663 |
|---|---|
| Device Name | Inbentus Versatile |
| Applicant | Iconic Solutions by Murcia, SL |
| Product Code | CBK · Anesthesiology |
| Decision Date | Apr 14, 2026 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 868.5895 |
| Device Class | Class 2 |
| Attributes | Therapeutic, Pediatric |
Indications for Use
The INBENTUS VERSATILE ventilator is intended to provide invasive and noninvasive ventilatory support to adult, pediatric, and neonatal patients. It is only intended for use by qualified health care personnel, within professional hospital facilities and to transport patients within those facilities.
Device Story
INBENTUS VERSATILE is a multi-purpose continuous ventilator providing invasive (via endotracheal/tracheal tube) and non-invasive (via mask) ventilatory support. It operates independently of hospital compressed air systems using an internal turbine for air and a compressed source for O2. The device features a 15.6-inch touchscreen monitor and is designed for use by qualified medical staff in hospital settings, including patient transport. It monitors respiratory parameters, waveforms, and loops, and provides high, medium, and low priority alarms. The device includes redundant mechanical safety systems to limit airway pressure and enable spontaneous breathing during power or pneumatic failure. It supports various ventilation modes (VC-CMV, VC-ACV, VC-SIMV, PC-CMV, PC-ACV, PC-SIMV, PC-APRV, SPN-CPAP) and maneuvers (inspiratory/expiratory hold, P0.1, PEEPi, O2 boost, recruitment, sigh). Clinical benefit is derived from providing life-sustaining respiratory support across diverse patient populations within hospital environments.
Clinical Evidence
Bench testing only. Evidence includes biocompatibility (ISO 18562-1/2/3), software verification/validation (IEC 62304), electrical/mechanical/thermal safety (IEC 60601-1, IEC 60601-1-2, IEC TR 60601-4-2), alarm safety (IEC 60601-1-8), critical care ventilator performance (ISO 80601-2-12), respiratory gas monitor performance (ISO 80601-2-55), waveform comparison tests, use-life reliability, and usability studies (IEC 62366-1).
Technological Characteristics
Ventilator with 15.6-inch touchscreen; internal turbine for air, external O2 source; AC/dual Li-ion battery power. Materials evaluated per ISO 18562. Standards: ISO 80601-2-12, ISO 80601-2-55, IEC 60601-1, IEC 60601-1-2, IEC 62304, IEC 62366-1. Connectivity: Not specified. Sterilization: Not specified.
Indications for Use
Indicated for invasive and noninvasive ventilatory support in adult, pediatric, and neonatal patients. Intended for use by qualified healthcare personnel in professional hospital facilities and for patient transport within those facilities.
Regulatory Classification
Identification
A continuous ventilator (respirator) is a device intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Adult, pediatric, and neonatal ventilators are included in this generic type of device.
Predicate Devices
- Hamilton-C6 (K201658)
Submission Summary (Full Text)
{0}
FDA U.S. FOOD & DRUG ADMINISTRATION
April 14, 2026
Iconic Solutions by Murcia, SL
% Dulciana Chan
Contract Consultant
RQM+
5000 Centregreen Way Suite 100, Cary, NC 27513 USA
Re: K252663
Trade/Device Name: INBENTUS VERSATILE
Regulation Number: 21 CFR 868.5895
Regulation Name: Continuous ventilator
Regulatory Class: Class II
Product Code: CBK
Dated: March 17, 2026
Received: March 17, 2026
Dear Dulciana Chan:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801; medical device reporting (reporting of medical device-related adverse events) (21 CFR 803) for devices
U.S. Food & Drug Administration
10903 New Hampshire Avenue
Silver Spring, MD 20993
www.fda.gov
{1}
K252663 - Dulciana Chan
Page 2
or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reporting-combination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Ethan L. Nyberg -S
Ethan Nyberg, Ph.D.
Assistant Director, Respiratory Devices Team
DHT1C: Division of Sleep Disordered Breathing, Respiratory and Anesthesia Devices
OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices
Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
{2}
FORM FDA 3881 (6/20)
Page 1 of 1
PSC Publishing Services (301) 443-6740
EF
| DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Indications for Use | Form Approved: OMB No. 0910-0120 Expiration Date: 06/30/2023 See PRA Statement below. |
| --- | --- |
| 510(k) Number (if known) K252663 | |
| Device Name INBENTUS VERSATILE | |
| Indications for Use (Describe) The INBENTUS VERSATILE ventilator is intended to provide invasive and noninvasive ventilatory support to adult, pediatric, and neonatal patients. It is only intended for use by qualified health care personnel, within professional hospital facilities and to transport patients within those facilities. | |
| Type of Use (Select one or both, as applicable) ☑ Prescription Use (Part 21 CFR 801 Subpart D) ☐ Over-The-Counter Use (21 CFR 801 Subpart C) | |
| CONTINUE ON A SEPARATE PAGE IF NEEDED. | |
| This section applies only to requirements of the Paperwork Reduction Act of 1995. *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* | |
| The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov | |
| "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." | |
{3}
INBENTUS MEDICAL TECHNOLOGY
# 510(k) SUMMARY
## DATE PREPARED
April 7, 2026
## MANUFACTURER AND 510(k) OWNER
ICONIC SOLUTIONS BY MURCIA, SL
Calle Central, 13, 1°C
30100, Murcia, Spain
Telephone: +34 968 96 52 72
Official Contact: Antonio Alarcón Miñarro, QA & RA Manager
## DEVICE INFORMATION
Proprietary Name/Trade Name: INBENTUS VERSATILE
Common Name: Continuous Ventilator
Regulation Number: 21 CFR 868.5895
Class: II
Product Code: CBK
Review Panel: Anesthesiology
## PREDICATE DEVICE IDENTIFICATION
The INBENTUS VERSATILE is substantially equivalent to the following predicate device:
| 510(k) Number | Predicate Device Name / Manufacturer | Primary Predicate |
| --- | --- | --- |
| K201658 | Hamilton-C6 / Hamilton Medical AG | ✓ |
## DEVICE DESCRIPTION
The INBENTUS VERSATILE is a multi-purpose ventilator for patients requiring ventilatory support. It is intended to be used only by qualified medical staff within professional hospital facilities, or by qualified medical staff during the transport of patients within the hospital facility. The INBENTUS VERSATILE ventilator is independent of hospital compressed air systems and can provide both invasive (via endotracheal tube) and non-invasive (via mask) ventilation for adult, pediatric, and neonatal patients throughout their hospital stay.
## INDICATIONS FOR USE
The INBENTUS VERSATILE ventilator is intended to provide invasive and noninvasive ventilatory support to adult, pediatric, and neonatal patients.
It is only intended for use by qualified health care personnel, within professional hospital facilities and to transport patients within those facilities.
## COMPARISON OF TECHNOLOGICAL CHARACTERISTICS
ICONIC SOLUTIONS BY MURCIA, SL believes that the INBENTUS VERSATILE is substantially equivalent to the predicate devices based on the information summarized here:
510(k) Summary
{4}
INBENTUS
MEDICAL TECHNOLOGY
The subject device has the same intended use as the primary predicate device cleared in K201658 and similar indications for use. Both devices are intended to be used in the same environment (i.e., healthcare facilities) and in the same patient populations (i.e., adult, pediatric and neonatal patients). The subject device has similar design and dimensions to the predicate device, and both devices include similar functions and performance specifications.
The main differences with the primary predicate are the absence of optional functionalities including high flow therapy, pulse oximetry, and capnography in the subject device. The absence of these functions does not impact the intended use and conditions of use of the device. The technological characteristics of the subject device have undergone testing to ensure the device is substantially equivalent to the predicate. A comparative summary of the technological characteristics of the subject and predicate device is presented in the table below.
| Technical Characteristic | Subject device: INBENTUS VERSATILE | Predicate device: Currently marketed HAMILTON-C6 K201658 | Comparison |
| --- | --- | --- | --- |
| Intended use | The INBENTUS VERSATILE ventilator is intended to provide invasive and non-invasive ventilatory support to adult, pediatric, and neonatal patients. It is only intended for use by qualified health care personnel, within professional hospital facilities and to transport patients within those facilities. | The HAMILTON-C6 ventilator is intended to provide positive pressure ventilatory support to adults and pediatrics and optionally infants and neonates. Intended areas of use:
• In the intensive care ward, intermediate care ward, emergency ward, long term acute care hospital or in the recovery room
• During transfer of ventilated patients within the hospital. The HAMILTON-C6 ventilator is a medical device intended for use by qualified, trained personnel under the direction of a physician and within the limits of its stated technical specifications. | Identical. |
| Product classification code | CBK | CBK | Identical. |
| CFR citation | 21 CFR 868.5895 | 21 CFR 868.5895 | Identical. |
510(k) Summary
{5}
INBENTUS
MEDICAL TECHNOLOGY
| Technical Characteristic | Subject device: INBENTUS VERSATILE | Predicate device: Currently marketed HAMILTON-C6 K201658 | Comparison |
| --- | --- | --- | --- |
| Principal operator | Qualified, trained personnel under the direction of a physician. | Qualified, trained personnel under the direction of a physician. | Identical. |
| Environment of use | To be used in professional hospital facilities and to transport patients within those facilities. | Intended areas of use: Health care facilities
During transfer of ventilated patients within health care facilities | Identical. |
| Intended patient population | Adult, pediatric, and neonatal patients. | Adults and pediatrics and optionally infants and neonates. | Identical. |
| Device Configuration | INBENTUS VERSATILE ventilator features a 15.6-inch touch screen monitor and a ventilation unit. The system is compact to adapt to different ICU configurations. | HAMILTON-C6 includes a 17-inch touchscreen panel and the ventilation unit.
HAMILTON-C6 offers flexible device configuration: mounted on trolley, shelf-mounted option... | Substantially Equivalent. |
| Method of supply gas pressurization | Internal turbine for air, compressed source for O2. | Internal turbine for air, compressed source for O2. | Identical. |
| Power source | AC.
Battery (x2). | AC.
Battery (x2) | Identical. |
| Battery | Lithium-ion
Up to 2.5h with 1 battery,
Up to 5h with 2 batteries. | Lithium-ion
> 1.5h 1 battery,
> 3h 2 batteries. | Substantially Equivalent. |
| Supply gas | High Pressure Oxygen, Ambient air. | High Pressure Oxygen, Ambient air. | Identical. |
| Therapy Types | Invasive ventilation
Non-invasive ventilation | Invasive,
Non-invasive,
HiFlowO2. | Substantially Equivalent.
High Flow Oxygen therapy not included in subject device. |
| Patient interface | Provide invasive ventilation (via endotracheal tube, ET o tracheal tube, TT tube) and non-invasive ventilation and breathing support (via mask). | Delivered invasively ventilation (via endotracheal tube, ET o tracheal tube, TT tube) or noninvasively (via mask). | Identical. |
510(k) Summary
{6}
INBENTUS
MEDICAL TECHNOLOGY
| Technical Characteristic | Subject device: INBENTUS VERSATILE | | | | Predicate device: Currently marketed HAMILTON-C6 K201658 | | | | Comparison |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Operating Ventilation Modes (For adults (A), pediatrics (P), and neonates (N)) | Mode | A | P | N | Mode | A | P | N | |
| | Invasive Ventilation | | | | | | | | |
| | VC-CMV | x | x | - | (S)CMV | x | x | - | SE |
| | VC-ACV | x | x | - | (S)CMV | x | x | - | SE |
| | VC-SIMV | x | x | - | SIMV | x | x | - | SE |
| | (PC-CMV)+PCVR | x | x | x | APVcmv/(S)CMV+ | x | x | x | SE |
| | (PC-ACV)+PCVR | x | x | x | APVcmv/(S)CMV+ | x | x | x | SE |
| | (PC-SIMV)+PCVR | x | x | x | APVsimv/SIMV+ | x | x | x | SE |
| | PC-CMV | x | x | x | PCV+ | x | x | x | SE |
| | PC-ACV | x | x | x | PCV+ | x | x | x | SE |
| | PC-SIMV | x | x | x | PSIMV+ | x | x | x | SE |
| | PC-SIMV+ | x | x | x | DouPAP | x | x | x | SE |
| | PC-APRV | x | x | x | APRV | x | x | x | SE |
| | SPN-CPAP | x | x | x | SPONT | x | x | x | SE |
| | -- | | | | ASV | o | o | | Not included in subject device |
| | Non-Invasive Ventilation | | | | | | | | |
| | (NIV) SPN-CPAP | x | x | x | NIV & nCPAP-PS | x | x | x | SE |
| | -- | x | x | x | NIV-ST | x | x | x | Not included in subject device |
| | Legend: x : Available; - : Not available; o : Optional | | | | | | | | |
| Performance | Conformance to ISO 80601-2-12 requirements on essential performance of critical care ventilators. Waveform comparison tests with predicate device. | | | | Conformance to ISO 80601-2-12 requirements on essential performance of critical care ventilators | | | | Substantially Equivalent |
| Device Safety Measures | In case of a power supply, technical, or pneumatics failure, the INBENTUS VERSATILE ventilator includes several redundant mechanical safety systems that allow for reducing and limiting airway | | | | In case of a power supply, technical, or pneumatics failure the ambient valve allows spontaneous breathing. | | | | Substantially equivalent |
510(k) Summary
{7}
INBENTUS
MEDICAL TECHNOLOGY
| Technical Characteristic | Subject device: INBENTUS VERSATILE | | | | Predicate device: Currently marketed HAMILTON-C6 K201658 | | | | Comparison |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | pressure and enabling the patient's spontaneous breathing | | | | | | | | |
| Calibrations and pre-operational checks | Compliance and leakage test | | | | Leakage Test | | | | Substantially equivalent |
| | Resistance Test | | | | Resistance Test (Step 1 of Patient Flow Sensor Test) | | | | Substantially equivalent |
| | Patient Flow Sensor Test (Two Steps) | | | | Patient Flow Sensor Test (Two Steps) | | | | Substantially equivalent |
| | Oxygen Concentration Sensor calibration Test | | | | Oxygen Concentration Sensor calibration Test | | | | Substantially equivalent |
| User Interface, Screens and functions | Alarm banner Alarm silence key Monitored Parameters Waveforms and Loops Events Log Screenshots, video, log | | | | Alarm message bar Alarm silence key Monitored Parameters Waveforms and Loops Events Logs Screenshots, log | | | | Substantially Equivalent |
| Alarms and monitoring | High, medium, and low alarm priorities Optical and acoustical alarm indication Adjustable alarm limits | | | | High, medium, and low alarm priorities Optical and acoustical alarm indication Adjustable alarm limits | | | | Substantially Equivalent |
| Tools and ventilation maneuvers | Mode | A | P | N | Mode | A | P | N | Comparison |
| | Inspiratory hold | x | x | x | Inspiratory hold | x | x | x | SE |
| | Expiratory hold | x | x | x | Expiratory hold | x | x | x | SE |
| | P0.1 Meas. | x | x | x | P0.1 Meas. | x | x | x | SE |
| | PEEPi Meas. | x | x | x | AutoPEEP Meas | x | x | x | SE |
| | O2 Boost | x | x | x | Oxygen Enrich. | x | x | x | SE |
| | Alveolar recr. | x | x | x | Recruitment | x | x | x | SE |
| | Sigh | x | x | - | Sigh | x | x | - | SE |
| | Legend: x : Available; - : Not available | | | | | | | | |
| Nebulizer | Pneumatic Nebulizer | | | | Pneumatic Nebulizer Electronic (Option) | | | | Substantially equivalent for included parts. |
| External devices and sensors options | Humidifier | | | | Electr. Controlled Hum.(Op) Intellicuff (Option) CO2 MainStream (Option) | | | | Substantially equivalent for included parts. |
510(k) Summary
{8}
INBENTUS
MEDICAL TECHNOLOGY
| Technical Characteristic | Subject device: INBENTUS VERSATILE | Predicate device: Currently marketed HAMILTON-C6 K201658 | Comparison |
| --- | --- | --- | --- |
| | | CO2 SideStream (Option)
SpO2 (Option) | |
# SUMMARY OF NON-CLINICAL TESTING
The following tests were performed to demonstrate substantial equivalence based on current industry standards.
## Biocompatibility:
Biocompatibility evaluation of the gas pathway was conducted according to ISO 18562-1 and FDA’s Biocompatibility Guidance. Testing included:
- Particulate matter (PM) emissions per ISO 18562-2
- Volatile organic compound (VOC) emissions per ISO18562-3
## Software/Cybersecurity:
Software verification and validation testing was performed per IEC 62304 Medical device software – Software life cycle processes to demonstrate safety and performance based on current industry standards.
## Electrical, Mechanical, and Thermal Safety, and Electromagnetic Compatibility:
The subject device has been designed to conform to the following standards covering electrical, mechanical, and thermal safety and EMC:
- IEC 60601-1
- IEC 60601-1-2
- IEC TR 60601-4-2
## Performance Testing:
The following tests were performed on the INBENTUS VERSATILE:
- System Level Performance Verification Testing
- Alarm Safety and Performance Testing per IEC 60601-1-8
- Basic Safety and Essential Performance of Critical Care Ventilators per ISO 80601-2-12
- Basic Safety and Essential Performance of Respiratory Gas Monitors per ISO 80601-2-55
- Waveform Comparison Test with predicate device
- Use-Life Reliability Testing
- Usability Study per IEC 62366-1
## CONCLUSION
Based on the testing performed including biocompatibility, software and cybersecurity, electrical safety, electromagnetic compatibility, usability and performance testing, it can be concluded that the subject device does not raise different questions of safety or effectiveness compared to the
510(k) Summary
{9}
INBENTUS
MEDICAL TECHNOLOGY
predicate device. The similar indications for use, technological characteristics, and performance characteristics for the proposed INBENTUS VERSATILE ventilator are assessed to be substantially equivalent to the primary predicate device.
510(k) Summary
7
