FDA Device Intelligence
Home › Cofoe Medical Technology Co.,Ltd › babaka

babaka

Cofoe Medical Technology Co.,Ltd · Model New E+ · UDI-DI 06950715503294

IPT
5
510(k) clearances
4
Adverse events (1 deaths)
0
Recalls
131
Facilities

Description

Back Brace

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.