FDA Device Intelligence
Home › Doppkon GmbH & Co. KG › N/A

N/A

Doppkon GmbH & Co. KG · Model A-001-230 · UDI-DI 04262494462573

HRT Prescription
0
510(k) clearances
21
Adverse events
0
Recalls
99
Facilities

Description

Tendon Stripper Closed OD 9.0 mm, WL 330mm

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.