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Bruder Karpecki

The Hilsinger Company Parent, Llc · Model 98656 · UDI-DI 00041533986560

HNW Prescription
3
510(k) clearances
50
Adverse events
0
Recalls
139
Facilities

Description

KARPECKI PUNCTAL DILATOR- DOUBLE ENDED

Query this across every FDA database — by API.

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.