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Tontarra Medizintechnik GmbH
Tontarra Medizintechnik GmbH · Model AR-210 · UDI-DI 04050183370182
KAL
Prescription
5
510(k) clearances
15
Adverse events
1
Recalls
123
Facilities
Description
Alar Retraktor
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-05-25 | TELEFLEX LLC | There are incomplete pre-cleaning instructions within the Instructions for Use (IFU). |
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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.