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Hybrid Dressing - Revo HFD-D1030

by Genadyne Biotechnologies Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00849405002697 UDI-DI Date12 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Hybrid Dressing - Revo
Generic Name
Negative-pressure wound therapy system foam dressing, non-antimicrobial
Model / Ref / Catalog
HFD-D1030
Primary DI / UDI-DI
00849405002697
FDA Product Code
OMP
GMDN Term
Negative-pressure wound therapy system foam dressing, non-antimicrobial
Device Class
Class II
Regulation Number
878.4780
GUDID distribution status
In Commercial Distribution

Other devices from Genadyne Biotechnologies Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No