Data / Medical devices / Japan / Nakamura Dental Handpiece MFG. Co., Ltd.
Nakamura Dental Handpiece MFG. Co., Ltd.: FDA-registered device maker in ITABASHI-KU Tokyo, Japan, 1 510(k) clearance
Nakamura Dental Handpiece MFG. Co., Ltd. is registered with the FDA (registration 9614686) in ITABASHI-KU Tokyo, Japan. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 20, 2008. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 9614686
- FEI number
- 3003340029
- Address
- 59-2 Minami-Cho, ITABASHI-KU Tokyo, Japan, 173-0027
- Owner or operator
- NAKAMURA DENTAL HANDPIECE MFG. CO., LTD. (9010791)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- March 21, 2008
- Registered through
- 2026
- Brand names listed
- ACCLEAN, CONTRA ANGLE, HyGenie, ND, Prophy Sport, ProphyPro, Quality Plus, TT(Turbo Torque)1000 Highspeed Airturbine Handpiece and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Handpiece, Air-Powered, Dental | EFB | 1 | Manufacturer | accessdata.fda.gov |
| Handpiece, Contra- And Right-Angle Attachment, Dental | EGS | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment | HWE | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 20, 2008 | K073652 | ND LOW SPEED AIRMOTOR AND HANDPIECE, HIGHSPEED AIRTURBINE HANDPIECE, E-TYPE STRAIGHT NOSECONE AND CONTRA ANGLE | EFB | Substantially Equivalent | Nakamura Magnifier Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Handpiece, Contra- And Right-Angle Attachment, Dental
- All makers of Handpiece, Air-Powered, Dental
- All makers of Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Updated March 20, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.