FDA Device Intelligence
Home › Rmo, Inc. › Schweickhardt

Schweickhardt

Rmo, Inc. · Model I00035 · UDI-DI 00885797610751

JEX Prescription
7
510(k) clearances
89
Adverse events
0
Recalls
235
Facilities

Description

3JAW EXPANSION BENDING PLIER UP TO 1.5MM

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.