Manufacturer registered with FDA
Osseo Pure Inc.
Lancaster, NY, United States. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 12
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Osseo Pure Inc. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | OSSEO PURE Cognac Prosthetic Screw M1.6x0.35OSSEO PURE Cognac Prosthetic Screw MUAOSSEO PURE Cognac Prosthetic Screw Structured PilasterOSSEO PURE Prosthetic Screw For Pilaster LongOSSEO PURE Prosthetic Screw For Pilaster ShortOSSEO PURE Retaining Screw Driver, Swivel LongOSSEO PURE Retaining Screw Driver, Swivel ShortOSSEO PURE Retaining Screw For Flat One LongOSSEO PURE Retaining Screw For MUA Conic Old StyleOSSEO PURE Retaining Screw For Pilaster TiBase 2 moreOSSEO PURE Spherical Prosthetic Screw MUA, LongOSSEO PURE Spherical Prosthetic Screw MUA, Short | 2024 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| OSSEO PURE INCFDA reg. 3030863060 | Lancaster, NY, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10090300). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.