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PreservaRidge™ Plug PRPSLM

by Collagen Matrix, Inc.

PreservaRidge™ Plug PRPSLM is a Class II device made by Collagen Matrix, Inc., listed in FDA GUDID since 17 Jan 2022 (UDI-DI 10813954024544), 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 Number10813954024544 UDI-DI Date17 Jan 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  • Withdrawn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
PreservaRidge™ Plug
Generic name
Dental bone void filling material, synthetic
Model / reference
PRPSLM
Primary DI / UDI-DI
10813954024544
FDA product code
NPM, LYC
GMDN term
Dental bone void filling material, synthetic
Device class
Class II
Regulation number
872.3930
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental bone matrix implant, synthetic

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Properties

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