Home › Clozex Medical, INC › Clozex Wound Closure
Clozex Wound Closure
Clozex Medical, INC · Model LK0150 · UDI-DI 00850019787108
0
510(k) clearances
5
Adverse events
1
Recalls
235
Facilities
Description
Laceration Kit 1 Closure: 50mm and Accessories
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-07 | INTEGRATED MEDCRAFT LLC | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
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.
