FDA Device Intelligence
Home › ENZTEC LIMITED › Bone Hook

Bone Hook

ENZTEC LIMITED · Model ME-BH0001 · UDI-DI 09421028119108

KIK
1
510(k) clearances
17
Adverse events
0
Recalls
116
Facilities

Description

A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure

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.