Neoss Implant System
Neoss AB · Model 64012 · UDI-DI 05060440330940
NPK
Prescription
10
510(k) clearances
83
Adverse events
1
Recalls
24
Facilities
Description
NeoGen® PTFE Membrane, Ti-Reinforced - L I
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-01 | Inion Ltd. | Aluminum pouch seal was noticed to be defective (slightly open). |
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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.