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Biopor® UMR-6052

by Ceremed, Inc.

Biopor® UMR-6052 is a Class II device made by Ceremed, Inc., listed in FDA GUDID since 20 Jul 2016 (UDI-DI UMR60520), 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 NumberUMR60520 UDI-DI Date20 Jul 2016ListedStatusListed 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  • Withdrawn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
Biopor®
Generic name
Polyethylene craniofacial tissue reconstructive material
Model / Ref / Catalog
UMR-6052
Primary DI / UDI-DI
UMR60520
FDA product code
KKY
GMDN term
Polyethylene craniofacial tissue reconstructive material
Device class
Class II
Regulation number
878.3500
GUDID distribution status
In Commercial Distribution
Size
Length — 50 Millimeter

Related devices

Category: Polyethylene craniofacial tissue reconstructive material

Other devices from Ceremed, Inc.

See all devices from Ceremed, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)