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PolyMem Silicone Border

by Ferris Mfg. Corp. 11 variants

PolyMem Silicone Border (2469) is a Class I device made by Ferris Mfg. Corp., listed in FDA GUDID since 14 Jan 2026 (UDI-DI 10735471024695), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10735471024695 UDI-DI Date14 Jan 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
PolyMem
Generic name
Wound-nonadherent dressing, absorbent, non-antimicrobial
Model / Ref / Catalog
Silicone Border, 2469
Primary DI / UDI-DI
10735471024695
FDA product code
NAD
GMDN term
Wound-nonadherent dressing, absorbent, non-antimicrobial
Device class
Class I
Regulation number
878.4020
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Similar devices

Other devices filed under FDA product code NAD (Dressing, Wound, Occlusive).

Other devices from Ferris Mfg. Corp.

See all devices from Ferris Mfg. Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Over-the-counter
  • Premarket exempt
Other properties (10, all answered No)