Geistlich Bio-Oss® Block

FDA UDI

Class II (US FDA UDI)

by Geistlich Pharma AG

Identity

Trade Name: Geistlich Bio-Oss® Block FDA UDI
Generic Name: Dental bone matrix implant, animal-derived FDA UDI
Model / Reference: 20131 FDA UDI

Identifiers

Primary DI / UDI-DI: 07610221010363 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

Dimensions & Sizes

Size: Depth — 1 Centimeter FDA UDI
Width — 1 Centimeter FDA UDI
Height — 2 Centimeter FDA UDI

Category: Dental bone matrix implant, animal-derived

Geistlich Bio-Oss® Block by Geistlich Pharma AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Geistlich Pharma AG

Sources (1)

FDA UDI 4ec2eb54-3b8d-4e23-9aa5-ed09dfc6e7c6 33 fields · synced May 30, 2026