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RETRACTOR

KLS-Martin L.P. · Model 01-001-06-07 · UDI-DI 00888118003232

EIG Prescription
8
510(k) clearances
34
Adverse events
0
Recalls
337
Facilities

Description

CHANNEL, KELLER, 10 MM TIP

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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.