FDA Device Intelligence
Home › DEROYAL INDUSTRIES, INC. › DeRoyal

DeRoyal

DEROYAL INDUSTRIES, INC. · Model OPB3433-T · UDI-DI 00749756774604

MRI Prescription
2
510(k) clearances
11
Adverse events
0
Recalls
162
Facilities

Description

BACK SUPPORT, O.S.O.

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.