Home › Spiggle & Theis Medizintechnik GmbH › Micro laryngeal forceps
Micro laryngeal forceps
Spiggle & Theis Medizintechnik GmbH · Model 50-516-03 · UDI-DI 04250676739070
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities
Description
round cups,conic. shaft distal 10° curv. upw., left curved, 23cm, irrig. channel
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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.