Neoss Implant System
Neoss AB · Model 64040 · UDI-DI 05060440335518
NPK
Prescription
10
510(k) clearances
83
Adverse events
1
Recalls
24
Facilities
Description
NeoGen Cape PTFE Membrane - M
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-01 | Inion Ltd. | Aluminum pouch seal was noticed to be defective (slightly open). |
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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.