FDA Device Intelligence
Home › Therafin Corporation › Dig-o-meter

Dig-o-meter

Therafin Corporation · Model 31900 · UDI-DI 00840252911828

IOD
10
510(k) clearances
169
Adverse events
0
Recalls
108
Facilities

Description

Dig-o-meter

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.