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Protech L
MEDITECH ENDOSCOPY LTD · Model INOV8-028L · UDI-DI 05060602250314
1
510(k) clearances
1
Adverse events
1
Recalls
9
Facilities
Description
ENDOSCOPIC STORAGE COVER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-12 | Healthmark Industries Co., Inc. | Product does not have FDA clearance. |
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.
