FDA Device Intelligence
Home › MEDLINE INDUSTRIES, INC. › BoneCam

BoneCam

MEDLINE INDUSTRIES, INC. · Model 08-20135 · UDI-DI 00818614021560

LXI Prescription
8
510(k) clearances
74
Adverse events
0
Recalls
43
Facilities

Description

BoneCam Angled Reusable Surgical Drill Guide

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.