Home › NOVO SURGICAL, INC. › Novo Surgical
Novo Surgical
NOVO SURGICAL, INC. · Model UR6280-22 · UDI-DI 00842331119040
EZO
Prescription
5
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities
Description
otis urethrotome, tip, conical
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.