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PuraFILL PFPLG625

by Collagen Matrix, Inc.

PuraFILL PFPLG625 is a Class II device made by Collagen Matrix, Inc., listed in FDA GUDID since 26 Mar 2025 (UDI-DI 00813954026732), 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 Number00813954026732 UDI-DI Date26 Mar 2025ListedStatusListed 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  • Withdrawn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
PuraFILL
Generic name
Dental bone void filling material, synthetic
Model / Ref / Catalog
PFPLG625
Primary DI / UDI-DI
00813954026732
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)