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Greven wire closing forceps

Spiggle & Theis Medizintechnik GmbH · Model 10-714-00 · UDI-DI 04250381848746

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510(k) clearances

Adverse events

Recalls

Facilities

Description

straight 0.8x5.0 mm, 8 cm

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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.