Data / Medical devices / United States / Dmi Technology LLC
Dmi Technology LLC: FDA-registered device maker in Lynbrook, NY, United States, 1 510(k) clearance
Dmi Technology LLC is registered with the FDA (registration 3030039110) in Lynbrook, NY, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 3, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030039110
- Address
- 67 N Prospect Ave, Lynbrook, NY, United States, 11563
- Owner or operator
- DMITechnology LLC (10089825)
- Roles
- Specification developer
- First device listed
- January 10, 2024
- Registered through
- 2026
- Brand names listed
- DMI Dental Implant System, DMI dental implant accessories, DMI dental implant drill bits
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Specification developer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Specification developer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Specification developer | accessdata.fda.gov |
| Non-Irrigation Endosseous Dental Implant Drill Bits | QRQ | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| October 3, 2016 | K160060 | DMi Dental Implant System | DZE | Substantially Equivalent | Dmi Innovative Medical Technology , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Non-Irrigation Endosseous Dental Implant Drill Bits
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
Updated October 3, 2016. 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.