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PuraFILL

FDA UDI

Class II (US FDA UDI)

by Collagen Matrix, Inc.

Identity

Trade Name
PuraFILL FDA UDI
Generic Name
Dental bone matrix implant, synthetic FDA UDI
Device Name
Bone Graft Composite Plug FDA UDI
Model / Reference
PFPLG625 FDA UDI
Description
Bone Graft Composite Plug FDA UDI

Identifiers

Catalog Number
PFPLG625 FDA UDI
Primary DI / UDI-DI
00813954026732 FDA UDI
FDA Product Code
NPM FDA UDI
LYC FDA UDI
GMDN Term
Dental bone matrix implant, synthetic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental bone matrix implant, synthetic

PuraFILL by Collagen Matrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental bone matrix implant, synthetic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa28a4bd-9a6e-4fee-8009-5b4b83cf4ce6 37 fields · synced Jun 6, 2026