Home › Institut Straumann AG › STRAUMANN MEMBRAGEL
STRAUMANN MEMBRAGEL
Institut Straumann AG · Model 1 · UDI-DI 07630031700148
NPK
Prescription
1
510(k) clearances
83
Adverse events
1
Recalls
24
Facilities
Description
Straumann® MembraGel® 0.8 ml
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-01 | Inion Ltd. | Aluminum pouch seal was noticed to be defective (slightly open). |
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.