Home › Spiggle & Theis Medizintechnik GmbH › Spoon curette, semi-sharp
Spoon curette, semi-sharp
Spiggle & Theis Medizintechnik GmbH · Model 90-201-07 · UDI-DI 04250381856017
JYG
Prescription
7
510(k) clearances
27
Adverse events
1
Recalls
148
Facilities
Description
curved upwards, with 5 mm bar 4 mm, 45°, bayonet, 27 cm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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.
