FDA Device Intelligence
Home › Richard Wolf GmbH › VERTEBRIS

VERTEBRIS

Richard Wolf GmbH · Model 892606036 · UDI-DI 04055207047002

HWK
1
510(k) clearances
132
Adverse events
0
Recalls
127
Facilities

Description

TREPHINE Ø 3.6MM WL 100MM sharp, reusable

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.