Home › AMERICAN MEDICAL ENDOSCOPY, INC. › Strauss Surgical
Strauss Surgical
AMERICAN MEDICAL ENDOSCOPY, INC. · Model STS-URO-711-01 · UDI-DI 00850033250893
5
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-22 | Olympus America Inc. | The device sterile package seal shows evidence of being breached or was breached |
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.
