FDA Device Intelligence
HomeKarl Storz GmbH & Co. KG › n.a.

n.a.

Karl Storz GmbH & Co. KG · Model 26055GP-S · UDI-DI 04048551393741

HIN Prescription
10
510(k) clearances
283
Adverse events (2 deaths)
0
Recalls
28
Facilities

Description

21FR BIPOLAR CUTTING LOOP

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.