FDA Device Intelligence
Home › KEELER LIMITED › 3.6V PROFESSIONAL SPOT RET & CASE

3.6V PROFESSIONAL SPOT RET & CASE

KEELER LIMITED · Model 1302-P-1009 · UDI-DI 05055272701587

HKL
6
510(k) clearances
0
Adverse events
0
Recalls
8
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.