FDA Device Intelligence
Home › Aesculap AG › activL®

activL®

Aesculap AG · Model FW915R · UDI-DI 04046963190859

QLQMJO Prescription
9
510(k) clearances
4
Adverse events
0
Recalls
15
Facilities

Description

ACTIV L LATERAL POSITIONER 0/45/90°

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.