Skip to content

PermeaDerm® PDB 15x30

by Stedical Scientific 3 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810125741104 UDI-DI Date3 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
PermeaDerm®
Generic Name
Animal-derived wound matrix dressing
Model / Ref / Catalog
PDB 15x30, B4153000
Primary DI / UDI-DI
00810125741104
510(k) Number
FDA Product Code
FRO
GMDN Term
Animal-derived wound matrix dressing
Device Class
U
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K153678)

Show all (12)

Other devices from Stedical Scientific

See all devices from Stedical Scientific →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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