Home › TITAN IMPLANT SYSTEMS, LLC › IDS Insight Dental Implant System
IDS Insight Dental Implant System
TITAN IMPLANT SYSTEMS, LLC · Model 540010 · UDI-DI 00855992007106
0
510(k) clearances
4
Adverse events
1
Recalls
0
Facilities
Description
5.4x10mm Bone Level Finished System
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-11-09 | Stryker Howmedica Osteonics Corp. | A review of packaging revealed the seal integrity of the pouch may be compromised. More specifically, there is a potential that the sterile pouch is not sealed at one end due to a |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
