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Coseal Surgical Sealant (Premixed)

by Angiotech Medical Device Technologies

PMA P010022

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 14 Dec 2001

PMA

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP010022 Date14 Dec 2001Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Trade Name
Coseal Surgical Sealant (Coseal)
Generic Name
Sealant, polymerizing
PMA Number
FDA Product Code
NBE
Device Class
Class III
Advisory Committee
General, Plastic Surgery
FDA Decision
APWD Approval withdrawn

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