Registered with FDA
ZimmerBiomet Americas DFE
Warsaw, IN, United States. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Costa Rica
Devices listed with FDA
What ZimmerBiomet Americas DFE currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Intraosseous Fixation ScrewDZL · Class 2 | Maxillofacial plates & screws | Lister | JUGGERKNOT MINI SOFT ANCHOR | 2020 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
ZimmerBiomet Americas DFE lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Biomet Sports Medicine (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 2 Oct 2014 | K140908 | JUGGERKNOT MINI SOFT ANCHOR | Biomet Sports Medicine | DZL Intraosseous Fixation Screw |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| Zimmer Biomet Centroamerica SAFDA reg. 3014315560 | san jose, Costa Rica | Foreign exporter |
Other names on FDA records
Zimmer Biomet Centroamerica SA
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10056779). 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.