FDA Device Intelligence
Home › Rmo, Inc. › 3D

3D

Rmo, Inc. · Model K00760 · UDI-DI 00885797100153

DYT Prescription
4
510(k) clearances
70
Adverse events
0
Recalls
90
Facilities

Description

3D LING ARCH ASST 30

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.