FDA Device Intelligence
Home › KEELER LIMITED › Cryomatic Console

Cryomatic Console

KEELER LIMITED · Model 2509-P-1000 · UDI-DI 05055272707633

HRN
10
510(k) clearances
3
Adverse events
0
Recalls
4
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.