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PDT, Inc.

PDT, INC. · Model T732 Stieglitz 30° Splinter Forcep · UDI-DI 00813677023230

EMD
2
510(k) clearances
9
Adverse events
0
Recalls
122
Facilities

Description

T732 Stieglitz 45° Splinter Forcep (Version or Model Number '30°' description is incorrect, Device Description '45°' is correct)

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.