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Agenasorb Powder, Surgical Dusting

by Intl. Management Services, Inc.

PMA P880089

Active United States

PMA

Valid until

No expiry

PMA approval is not time-limited

FDA recalls

None found

in data synced 6 Oct 2026

Documents

PMA P880089↗

FDA record

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 PMAAPPR Approved NumberP880089 Date13 Sep 1990ApprovedStatusActive

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  • Withdrawn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 Active

Specification

PMA

Full name
Agenasorb
Generic Name
Powder, dusting, surgical
PMA Number
FDA Product Code
KGP
Advisory Committee
General, Plastic Surgery
FDA Decision
APPR Approved

Overview

AI-generated summary, 18 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

Agenasorb Powder is a surgical dusting powder classified as a Powder, dusting, surgical under FDA nomenclature. It is designed to reduce friction and tissue adhesion during surgical procedures, particularly in plastic surgery applications, by providing a smooth, dry surface on instruments and tissues.

This product is supplied as a sterile, single-use powder and is intended for use in operating room settings. It is regulated under an FDA Premarket Approval (PMA) with PMA Number P880089, and its use is categorized under the KGP product code. Storage and handling must comply with sterile medical device protocols.

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