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Antrum curette

Spiggle & Theis Medizintechnik GmbH · Model 30-205-03 · UDI-DI 04250381813201

JYG Prescription
7
510(k) clearances
27
Adverse events
1
Recalls
148
Facilities

Description

oval, large, 45° angled 4.0x9.0 mm

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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Data 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.