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Asclepii Poseidon Nanosilver Hydrogel OTC 3oz 1100073

by Asclepii 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 Number00735549200733 UDI-DIDate4 Dec 2025ListedStatusListed 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  • Withdrawn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
Asclepii Poseidon Nanosilver Hydrogel OTC 3oz
Generic Name
Wound hydrogel dressing, antimicrobial
Model / Reference
1100073
Primary DI / UDI-DI
00735549200733
510(k) Number
FDA Product Code
FRO
GMDN Term
Wound hydrogel dressing, antimicrobial
Device Class
U
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K131176)

Other devices from Asclepii Inc.

Properties

  • Over-the-Counter
  • Combination Product
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No