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Stryker GmbH · Model 915-1002 · UDI-DI 00886385024554

GEG Prescription
10
510(k) clearances
39
Adverse events
0
Recalls
228
Facilities

Description

Periosteal Elevator, straight edge

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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.