Newport Biologics Bone Graft Putty Mineral Collagen Composite

FDA UDI

Class II (US FDA UDI)

by Prismatik Dentalcraft, Inc.

Identity

Trade Name: Newport Biologics Bone Graft Putty Mineral Collagen Composite FDA UDI
Generic Name: Dental bone matrix implant, synthetic FDA UDI
Device Name: Bone Graft Putty Mineral Collagen Composite FDA UDI
Model / Reference: 70-BIO-BGP20 FDA UDI
Description: Bone Graft Putty Mineral Collagen Composite FDA UDI

Identifiers

Catalog Number: 70-BIO-BGP20 FDA UDI
Primary DI / UDI-DI: D74570BIOBGP200 FDA UDI
FDA Product Code: LYC FDA UDI
NPM 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental bone matrix implant, synthetic

Newport Biologics Bone Graft Putty Mineral Collagen Composite by Prismatik Dentalcraft, Inc. — Class II — FDA UDI — listed in FDA GUDID

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Prismatik Dentalcraft, Inc.

Sources (1)

FDA UDI 123dc82e-86d5-456a-9967-e940ba9b1b48 36 fields · synced May 31, 2026