Skip to content

Bonvadis Topical Cream Post-Surgical

by Oneness Biotech Co., Ltd. 2 variants

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 Number04719883980380 UDI-DI Date20 Mar 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  • Withdrawn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
Bonvadis Topical Cream
Generic Name
Skin osmotic dressing, non-antimicrobial
Model / Reference
Post-Surgical
Primary DI / UDI-DI
04719883980380
FDA Product Code
FRO
GMDN Term
Skin osmotic dressing, non-antimicrobial
Device Class
U
GUDID distribution status
In Commercial Distribution
Size
Weight — 3 Gram

Other devices from Oneness Biotech Co., Ltd.

See all devices from Oneness Biotech Co., Ltd. →

Properties

  • Prescription Use
  • Combination Product
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No