FDA Device Intelligence
Home › Heine Optotechnik GmbH & Co. KG › HEINE SIGMA®250

HEINE SIGMA®250

Heine Optotechnik GmbH & Co. KG · Model 000 · UDI-DI 04053755126347

GCM
10
510(k) clearances
1,495
Adverse events (1 deaths)
0
Recalls
20
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.