FDA Device Intelligence
Home › Shenzhen Fitfaith Technology Co., Ltd › Fitfaith

Fitfaith

Shenzhen Fitfaith Technology Co., Ltd · Model M130E · UDI-DI 06970953260063

PGJ
0
510(k) clearances
2
Adverse events
0
Recalls
37
Facilities

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.