Data / Medical devices / United States / Kat Implants, LLC
Kat Implants, LLC: FDA-registered device maker in Portsmouth, NH, United States, 2 510(k) clearances
Kat Implants, LLC is registered with the FDA (registration 3007728094) in Portsmouth, NH, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 23, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007728094
- Address
- 222 International Drive, No. 185, Portsmouth, NH, United States, 03801
- Owner or operator
- KAT Implants, LLC (10028730)
- Roles
- Manufacturer
- First device listed
- March 1, 2009
- Registered through
- 2026
- Brand names listed
- Abutment SR 2.7, Abutment SR 20º, Abutment SR 3.5, Angle Abutment 4.2 10º, Angle Abutment 4.2 20º, Angle Abutment 4.6 10º, Angle Abutment 4.6 20º, Angle Abutment 5 10º and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | 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 |
|---|---|---|---|---|---|---|
| February 23, 2012 | K112758 | KAT IMPLANTS SYSTEM ONE-PIECE IMPLANTS 2.5X10 | DZE | Substantially Equivalent | Kat Implants, LLC | accessdata.fda.gov |
| February 2, 2009 | K083544 | KAT IMPLANT SYSTEM | NHA | Substantially Equivalent | Kat Implants, LLC | accessdata.fda.gov |
Compare with other makers
Updated February 23, 2012. 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.