FDA Device Intelligence
Home › DESARROLLO E INVESTIGACION MEDICA ARAGONESA SL › Anchorsure

Anchorsure

DESARROLLO E INVESTIGACION MEDICA ARAGONESA SL · Model A-SURE02 · UDI-DI 08436568350141

PBQ
8
510(k) clearances
64
Adverse events
1
Recalls
9
Facilities

Recalls

DateFirmReason
2021-12-13FEMSelect LtdCertain lots may not have been packaged wth the Channel Tube Limiter.

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.