FDA Device Intelligence
Home › Gyrus ACMI, LLC › GYRUS ACMI, INC

GYRUS ACMI, INC

Gyrus ACMI, LLC · Model 140867 · UDI-DI 00821925015548

FZD Prescription
1
510(k) clearances
11
Adverse events
0
Recalls
5
Facilities

Description

MEDIUM CANAL WALL PROSTHESIS POROUS HYDROXYLAPATITE

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.