The Dental Handpiece Cleaner and Lubricant is intended to be used during routine maintenance in order to lubricate and clean air-powered Dental Handpieces (including low speed and high speed) and Dental air motors after each patient use and prior to sterilization. The Dental Handpiece Lubricant is intended to be used during routine maintenance in order to lubricate air-powered Dental Handpieces (including low speed and high speed) and Dental air motors after each patient use and prior to sterilization.
Device Story
Aerosol and liquid maintenance products for air-powered dental handpieces; used in dental clinics by staff. Products contain mineral oil and isopropyl alcohol (aerosol versions) or refined mineral oil (lubricant version). Applied by spraying into air drive tube or dropping into tube; air pressure delivers lubricant to internal bearings, gears, and auto chucks. Removes contamination and reduces friction; ensures proper handpiece function; supports maintenance protocols prior to sterilization. Benefits include extended device life and consistent performance.
Clinical Evidence
No clinical data; substantial equivalence supported by bench testing comparing subject devices to predicate. Bench tests evaluated bur extraction force, concentricity, noise level, and torque, demonstrating performance equivalent to the predicate.
Technological Characteristics
Aerosol and liquid formulations. Aerosol contains mineral oil, isopropyl alcohol, and propellants (propane/n-butane). Lubricant contains 100% refined mineral oil. Insoluble in water. Applied via air drive tube. Class I device, 21 CFR 872.4200.
Indications for Use
Indicated for routine maintenance, cleaning, and lubrication of air-powered dental handpieces (low and high speed) and dental air motors after patient use and prior to sterilization.
Regulatory Classification
Identification
A dental handpiece and accessories is an AC-powered, water-powered, air-powered, or belt-driven, hand-held device that may include a foot controller for regulation of speed and direction of rotation or a contra-angle attachment for difficult to reach areas intended to prepare dental cavities for restorations, such as fillings, and for cleaning teeth.
Predicate Devices
PANA SPRAY lubricant oil by NSK America Corp. (K052700)
Related Devices
K163483 — PANA SPRAY Plus · Nakanishi, Inc. · Aug 15, 2017
K052700 — PANA-SPRAY · Nsk America Corp. · Dec 20, 2005
K173920 — LS OIL · J. Morita USA, Inc. · Oct 11, 2018
K131014 — PANA SPRAY PLUS · Nsk America Corp. · Aug 12, 2013
K070074 — LUBRINA, MODEL HIM-1 · J. Morita USA, Inc. · May 31, 2007
Submission Summary (Full Text)
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K113674
Image /page/0/Picture/2 description: The image shows the words "Handpiece Headquarters" in a bold, stylized font. Above the words is a line graph. The text is the main focus of the image.
A Henry Schein® COMPANY
### 510(K) SUMMARY:
- a- Submitted by: HANDPIECE HEADQUARTERS 620 S. Placentia Ave., Placentia CA 92870 Tel. 714-579-0175 Fax. 714-579-0186
- b- Contact person: Tina Steffanie-Oak, Tel. 717-335-7230, ext. 4150 Fax. 717-335-7240 Email: tina.steffanie-oak@henryschein.com
### c- Date summary prepared: 04/2/2012
### d- Device Name:
| Common Name: | Dental Handpiece and Accessories, Dental Handpiece Cleaner and<br>Lubricant. |
|----------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Trade Name: | Spray & Clean Handpiece Cleaner & Lubricant<br>Maxima Handpiece Cleaner & Lubricant<br>EZCARE Handpiece Cleaner & Lubricant<br>(3 trade names carry the same chemical formula ) |
| Common Name: | Dental Handpiece and Accessories, Dental Handpiece Lubricant. |
| Trade Name: | Maxima Handpiece Lubricant |
| Classification Name: | Class I Device, 21 CFR 872.4200, Handpiece, Air-power<br>Dental, EFB |
e- Substantial Equivalency is claimed against the following devices: PANA SPRAY lubricant oil by NSK America Corp. - K052700
f- Description of the device:
Dental Handpiece Cleaner and Lubricant (Spray & Clean Handpiece Cleaner & Lubricant, Maxima Handpiece Cleaner & Lubricant, and EZcare Handpiece Cleaner & Lubricant), This is an aerosol product that is used during routine maintenance. It contains two major components, which are Mineral oil and Isopropyl Alcohol. The product lubricates and cleans dental handpieces and air motors when sprayed directly into the air drive tube. It lubricates and cleans out contamination from all internal parts, such as the bearings, gears and auto chucks.
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# Dental Handpiece Lubricant: Maxima Handpiece Lubricant
Maxima Handpiece Lubricant contains mineral oil that drops directly into the air drive tube of the dental handpiece. When the user operates the handpiece, the pressure of air in the air drive tube will deliver the oil into the handpiece to lubricate the bearings, gears, and auto chucks.
# g- Statement of Intended Use:
The Dental Handpiece Cleaner and Lubricant is intended to be used during routine maintenance in order to lubricate and clean air-powered Dental Handpieces (including low speed and high speed) and Dental air motors after each patient use and prior to sterilization.
The Dental Handpiece Lubricant is intended to be used during routine maintenance in order to lubricate air-powered Dental Handpieces (including low speed and high speed) and Dental air motors after each patient use and prior to sterilization.
## h - Device and Predicate Comparison Table:
| Descriptive<br>Information | Subject Device: | Predicate: |
|--------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------|
| | Spray & Clean Handpiece Cleaner &<br>Lubricant, Maxima Handpiece<br>Cleaner & Lubricant, and EZCARE<br>Handpiece Cleaner & Lubricant<br><br>Maxima Handpiece Lubricant | NSK PANA SPRAY<br>LUBRICANT OIL SUPERIOR<br>CLEANING &LUBRICANT<br><br>NSK PANA SPRAY<br>LUBRICANT OIL SUPERIOR<br>CLEANING &LUBRICANT |
| Indication of use | The Dental Handpiece Cleaner and<br>Lubricant is intended to be used<br>during routine maintenance in order to<br>lubricate and clean air-powered<br>Dental Handpieces (including low<br>speed and high speed) and Dental air<br>motors after each patient use and<br>prior to sterilization.<br><br>The Dental Handpiece Lubricant is<br>intended to be used during routine<br>maintenance in order to lubricate air-<br>powered Dental Handpieces<br>(including low speed and high speed)<br>and Dental air motors after each<br>patient use and prior to sterilization. | This new device is a lubricant<br>and is intended for use to clean<br>and lubricate the dental and<br>medical surgical handpieces. |
| Components<br>name/<br>Weight<br>percentage<br>(% w/w) | Spray & Clean Handpiece Cleaner &<br>Lubricant, Maxima Handpiece<br>Cleaner & Lubricant, and EZCARE<br>Handpiece Cleaner & Lubricant<br>(3 trade names carry the same<br>chemical formula )<br>Propellant: (84% w/w)<br>Propane 7.5%<br>n-Butane 17.5%<br>Isopropanol 59% | PANA SPRAY<br><br>Propellant: (63% w/w)<br>Propane<br>Isobutane<br>n-Butane |
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| | Lubricant: (16% w/w)<br>Mineral oil 16%<br>Hydrocarbon Range C16-C28 0% | Lubricant: (16% w/w)<br>Petroleum Oil<br>Hydrocarbon Range C16-C28 |
|-----------|--------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------|
| | Maxima Handpiece Lubricant<br>Lubricant: (100% w/w)<br>Severely refined Mineral oil 100%<br>Hydrocarbon Range C16-C28 0% | Lubricant: (16% w/w)<br>Petroleum Oil<br>Hydrocarbon Range C16-C28 |
| Fragrance | N/A | N/A |
# Physical Property comparison table:
| Physical property | Predicate Device:<br>Pana Spray Lubricant Oil | Subject Device:<br>Spray & Clean Handpiece<br>Cleaner and Lubricant | Subject Device:<br>Maxima Handpiece<br>Lubricant |
|---------------------|-----------------------------------------------|---------------------------------------------------------------------|--------------------------------------------------|
| Physical State | Aerosol Product | Aerosol Product | Transparent Water-white Liquid |
| Color | clear | Clear | Clear |
| Solubility in Water | Insoluble | Insoluble | Insoluble |
| Specific Gravity | $0.63 \ (H_2O=1)$ | .70-.90 g/cc | $0.835 @ 15.6 \degree C \ (H_2O=1)$ |
| Boiling Point | -44 deg F-31 deg F | Propellant: 7.29 °F<br>Concentrate: 180 °F | 310 °C (590 °F) |
| Viscosity | n/a | n/a | n/a |
# i - Description of Non-Clinical Test Data used to support SE Decision:
The table below provides a general summary of the performance testing which was conducted on the subject devices and the predicate device. The testing results indicate that the subject devices meet their design performance requirements.
| Comparison | Test | Method | Conclusion |
|----------------------------------------------------------------------------|-------------------------------------|-----------------------------------------------------------------------------|-----------------------------------------------|
| Spray & Clean<br>Handpiece<br>Cleaner &<br>Lubricant vs.<br>NSK Pana Spray | Handpiece<br>Performance<br>Testing | Cycle<br>Bur extraction force,<br>concentricity, noise<br>level, and torque | Met handpiece<br>performance<br>specification |
| Maxima<br>Handpiece<br>Lubricant vs.<br>NSK Pana Spray | Handpiece<br>Performance<br>Testing | Cycle<br>Bur extraction force,<br>concentricity, noise<br>level, and torque | Met handpiece<br>performance<br>specification |
# j - Description of Clinical Test Data used to support SE Decision:
Clinical test data was not required to support our substantial equivalence determination.
# k - Conclusions Drawn from Non-Clinical Data:
Based on the information provided in this submission Handpiece Headquarters believes that the Dental Handpiece Cleaner & Lubricant and Dental Handpiece Lubricant are intended for the same use and are substantially equivalent to the predicate devices identified.
{3}------------------------------------------------
l – Biocompatibility: Biocompatibility testing has not been conducted on the subject devices, because the chemical components have already been incorporated in legally marketed devices with similar conditions of use and have a demonstrated history of biocompatibility.
{4}------------------------------------------------
# DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/4/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three lines forming its body and wings. The eagle is enclosed in a circle with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" around the perimeter.
#### Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Ms. Tina Steffanie-Oak Consultant Handpiece Headquarters Inc, - HPR Inc. 620 S. Placentia Avenue Placentia, California 92870
APR - 5 2012
Re: K113674
Trade/Device Name: Dental Handpiece Cleaner and Lubricant, and a Dental Handpiece Lubricant (sold under these brand names Spray & Clean Handpiece Cleaner & Lubricant, Maxima Handpiece Cleaner & Lubricant, EZcare Handpiece Cleaner & Lubricant, and Maxima Handpiece Lubricant)
Regulation Number: 21 CFR 872.4200
Regulation Name: Dental Handpiece and Accessories
Regulatory Class: I
Product Code: EFB
Dated: April 2, 2012
Received: April 3, 2012
Dear Ms. Steffanie-Oak:
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. 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.
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## Page 2 - Ms. Steffanie-Oak
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); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices /ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.
Sincerely yours,
Nh for
Anthony D. Watson, B.S., M.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
#### Enclosure
{6}------------------------------------------------
Indications for Use
113672
510(k) Number (if known):
Device Name: Dental Handpiece Cleaner and Lubricant, and a Dental Handpiece Lubricant (sold under these brand names Spray & Clean Handpiece Cleaner & Lubricant, Maxima Handpiece Cleaner & Lubricant, EZcare Handpiece Cleaner & Lubricant, and Maxima Handpiece Lubricant)
Indications for Use:
The Dental Handpiece Cleaner and Lubricant is intended to be used during routine maintenance in order to lubricate and clean air-powered Dental Handpieces (including low speed and high speed) and Dental air motors after each patient use and prior to sterilization.
The Dental Handpiece Lubricant is intended to be used during routine maintenance in order to lubricate air-powered Dental Handpieces (including low speed and high speed) and Dental air motors after each patient use and prior to sterilization.
Prescription Use X (Per 21 CFR 801 Subpart D) Subpart C)
AND/OR
Over-The-Counter Use
(Per 21 CFR 801
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Othuraltneen for MSR
Page 1 of 1
(Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices
510(k) Number: _______________________________________________________________________________________________________________________________________________________________
Panel 1
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