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Plena Flex CDMPP3040

by Collagen Matrix, Inc. 2 variants

Plena Flex CDMPP3040 is a Class II device made by Collagen Matrix, Inc., listed in FDA GUDID since 11 Mar 2022 (UDI-DI 00813954024615), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813954024615 UDI-DI Date11 Mar 2022ListedStatusListed 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  • Withdrawn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
Plena Flex
Generic name
Collagen dental regeneration membrane
Model / reference
CDMPP3040
Primary DI / UDI-DI
00813954024615
FDA product code
NPL
GMDN term
Collagen dental regeneration membrane
Device class
Class II
Regulation number
872.3930
GUDID distribution status
In Commercial Distribution

Related devices

Category: Collagen dental regeneration membrane

Similar devices in this category

Other devices filed under Collagen dental regeneration membrane.

Other devices from Collagen Matrix, Inc.

See all devices from Collagen Matrix, Inc. →

Properties

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