Not currently registered with FDA under this name
Straumann USA (On Behalf of Institut Straumann Ag)
Andover, MA, United States. Named as applicant on 2 dental 510(k) clearances between 2007 and 2010. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 22007–2010
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Straumann USA (On Behalf of Institut Straumann Ag) as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 16 Dec 2010 | K101956 | STRAUMANN MEMBRAGEL | NPK Intraoral Synthetic Barrier |
| 26 Sep 2007 | K071919 | P.004 ABUTMENTS | NHA Endosseous Dental Implant Abutment |
Some of these clearances are listed with FDA today by another company: Institut Straumann AG (1).
Sources
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 of the most recent filing, which can be a US agent.