SalvinOSS™ Xenograft Bone Graft Material

FDA UDI

Class II (US FDA UDI)

by Dsm Biomedical, Inc.

Identity

Trade Name: SalvinOSS™ Xenograft Bone Graft Material FDA UDI
Generic Name: Dental bone matrix implant, animal-derived FDA UDI
Device Name: Porcine Anorganic Dental Bone Graft FDA UDI
Model / Reference: 30070-01 FDA UDI
Description: Porcine Anorganic Dental Bone Graft FDA UDI

Identifiers

Catalog Number: SALVINOSS-0.50 FDA UDI
Primary DI / UDI-DI: 00812337027045 FDA UDI
FDA Product Code: NPM FDA UDI
GMDN Term: Dental bone matrix implant, animal-derived 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, animal-derived

SalvinOSS™ Xenograft Bone Graft Material by Dsm Biomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Dental bone matrix implant, animal-derived.

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Instradent XenoGraft — Nibec Co., Ltd. · Class II
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naturesQue MaxOss P — COLLAGEN MATRIX, INC. · Class II
BoneMedik-DM, 2~4mm, 5cc — Meta Biomed, Inc. · Class II
MinerOss® X — ACE SURGICAL SUPPLY CO., INC. · Class II

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: Dsm Biomedical, Inc.

Sources (1)

FDA UDI 469356f2-41e9-4a89-931b-ea662ebc1a8e 35 fields · synced May 31, 2026