← Product Code [HRS](/productcode/HRS) · K262649 # Alians Forearm (K262649) _Newclip Technics · HRS · Sep 28, 2026 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/device/K262649 ## Device Facts - **Applicant:** Newclip Technics - **Product Code:** [HRS](/productcode/HRS.md) - **Decision Date:** Sep 28, 2026 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3030 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Indications for Use The implants of the Alians Forearm range are indicated for the fixation of fractures and osteotomies of the radius and the ulna. ## Device Story Alians Forearm range consists of metallic plates and screws for orthopedic fracture fixation and osteotomies of radius and ulna; used by surgeons in clinical settings; implants provide mechanical stabilization of bone segments; provided sterile or non-sterile for hospital-based sterilization; device functions as traditional bone fixation hardware; clinical benefit includes stabilization of bone to facilitate healing. ## Clinical Evidence No clinical studies were performed. Evidence is based on bench testing and engineering analysis. ## Technological Characteristics Materials: Titanium alloy Ti-6Al-4V ELI (ASTM F136, ISO 5832-3). Principle: Metallic bone fixation plates and screws. Sterilization: Gamma or healthcare facility steam sterilization. Design: Standard orthopedic fixation hardware. ## Regulatory Identification Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system. ## Predicate Devices - TriMed Elbow & Forearm System - Forearm Plate ([K243987](/device/K243987.md)) - TriMed Ulnar Osteotomy Compression Plate ([K043263](/device/K043263.md)) - DEPUY / SYNTHES Small Fragment LCP System ([K011335](/device/K011335.md)) ## Reference Devices - Activmotion S range of Newclip Technics ([K241539](/device/K241539.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0} FDA U.S. FOOD & DRUG ADMINISTRATION September 28, 2026 Newclip Technics % J.D. Webb President The OrthoMedix Group, Inc. 4313 W. 3800 S. West Haven, Utah 84401 Re: K262649 Trade/Device Name: Alians Forearm Regulation Number: 21 CFR 888.3030 Regulation Name: Single/Multiple Component Metallic Bone Fixation Appliances And Accessories Regulatory Class: Class II Product Code: HRS, HWC Dated: July 29, 2026 Received: July 30, 2026 Dear J.D. Webb: 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 (the 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 available 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. Before making any change significantly affecting the safety or effectiveness of the device, you must submit a new premarket notification in accordance with 21 CFR 807.81. Additional information about changes that U.S. Food & Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993 www.fda.gov {1} K262649 - J.D. Webb Page 2 may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download). Your device is also subject to, among other requirements, the Quality Management System Regulation (QMSR) (21 CFR Part 820), which includes, but is not limited to, ISO 13485 clause 7.3 (Design controls), ISO 13485 clause 8.3 (Nonconforming product), ISO 13485 clause 8.5.2 (Corrective action), and ISO 13485 clause 8.5.3 (Preventative action). Please note that regardless of whether a change requires premarket review, the QMSR requires device manufacturers to review and approve changes to device design and production (ISO 13485 clause 7.3 and ISO 13485 clause 7.5) and document changes and approvals in the Medical Device File (ISO 13485 clause 4.2.3). 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 Part 803) for devices or postmarketing safety reporting (21 CFR Part 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 Management System Regulation (QMSR) (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050. All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/unique-device-identification-system-udi-system. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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- {2} K262649 - J.D. Webb Page 3 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, Christopher Ferreira, M.S. Assistant Director DHT6C: Division of Restorative, Repair, and Trauma Devices OHT6: Office of Orthopedic Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {3} | Indications for Use | | | | --- | --- | --- | | Please type in the marketing application/submission number, if it is known. This textbox will be left blank for original applications/submissions. | K262649 | ? | | Please provide the device trade name(s). | | ? | | Alians Forearm | | | | Please provide your Indications for Use below. | | ? | | The implants of the Alians Forearm range are indicated for the fixation of fractures and osteotomies of the radius and the ulna. | | | | Please select the types of uses (select one or both, as applicable). | ☑ Prescription Use (21 CFR 801 Subpart D) ☐ Over-The-Counter Use (21 CFR 801 Subpart C) | ? | {4} K262649 nct NEWCLIP-TECHNICS ## 510 (k) Summary Alians Forearm In accordance with 21 CFR 807.92 of the Federal Code of Regulations, the following 510(k) summary is submitted for the Alians Forearm range. # 1. Submitter: NEWCLIP TECHNICS P.A. de la Lande Saint Martin 45 rue des Garottières F-44115 Haute-Goulaine - France Telephone: (33) 2 28 21 37 12 # Contact Person: J.D. Webb The OrthoMedix Group, Inc. 4313 W. 3800 S. West Haven. UT 84401 Telephone: 512-590-5810 # 2. Trade name: Alians Forearm Common Name: Plate, Fixation, Bone / Screw, Fixation, bone Product code: HRS - Plate, Fixation, Bone HWC - Screw, Fixation, Bone Classification Name: Single/multiple component metallic bone fixation appliances and accessories. (21 CFR part. 888.3030) Smooth or threaded metallic bone fixation fastener.(21 CFR part. 888.3040) # 3. Primary and additional predicates or legally marketed devices which are substantially equivalent: - TriMed Elbow & Forearm System - Forearm Plate (K243987) - Primary Predicate Device - TriMed Ulnar Osteotomy Compression Plate (K043263) - Additional Predicate Device - DEPUY / SYNTHES Small Fragment LCP System (K011335) - Additional Predicate Device # Reference devices: - Activmotion S range of Newclip Technics (K241539, cleared on July 30th 2024) Page 1 of 3 {5} K262649 nct NEWCLIP-TECHNICS #### 4. Description of the device: The Alians Forearm range consists of plates and screws designed for the fixation of fractures and osteotomies of the radius and the ulna. The plates and screws of the Alians Forearm range will be provided sterile by gamma sterilization or non-sterile for sterilization by health care professionals prior to use. The instruments of the Alians Forearm range will be provided non-sterile for sterilization by health care professionals prior to use. #### Materials: Titanium alloy Ti-6Al-4V ELI (conform to ASTM F136 and ISO 5832-3) for the plates and screws. #### Function: The implants of the Alians Forearm range are indicated for the fixation of fractures and osteotomies of the radius and the ulna. #### 5. Indication for use The implants of the Alians Forearm range are indicated for the fixation of fractures and osteotomies of the radius and the ulna. #### 6. Summary of the technological characteristics compared to predicate The Alians Forearm range is substantially equivalent to the predicate devices in intended use, design, manufactured materials, and mechanical performance. The following tests and analyses were conducted: - Engineering analysis and static testing were performed on the worst-case plate in accordance with ASTM F382, with the results compared to the minimum performance criteria specified in the FDA Guidance - Orthopedic Fracture Fixation Plates – Performance Criteria for Safety and Performance Based Pathway (2022). - Torsional strength and driving torque were performed on the worst-case screw in accordance with ASTM F543, with the results evaluated against the minimum performance criteria specified in FDA's Guidance document, Orthopedic Non-Spinal Metallic Bone Screws and Washers – Performance Criteria for Safety and Performance Based Pathway (2024). Page 2 of 3 {6} K262649 [LOGO] - Pullout strength was evaluated through engineering analysis using the Chapman (1996) equation, as specified in the FDA Guidance, with the results evaluated against the guidance's minimum acceptable values. ### 7. Clinical Test Summary: No clinical studies were performed. ### 8. Conclusions: Newclip Technics considers the Alians Forearm range to be equivalent to the predicate devices listed above. This conclusion is based upon the device's similarities in principles of operation, technology, materials, and indications for use. Page 3 of 3 --- **Source:** [https://fda.innolitics.com/device/K262649](https://fda.innolitics.com/device/K262649) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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