← Back to catalogue

Osseo Seal

FDA UDI

Class II (US FDA UDI)

by Odontit S.a.

Identity

Trade Name
Osseo Seal FDA UDI
Generic Name
Dental bone matrix implant, animal-derived FDA UDI
Device Name
Osseo Seal 0.5 cc Bovine bone graft 250-1000 micron vial FDA UDI
Model / Reference
OSS-1000-05 FDA UDI
Description
Osseo Seal 0.5 cc Bovine bone graft 250-1000 micron vial FDA UDI

Identifiers

Primary DI / UDI-DI
D914OSS100005 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

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

Yes

FDA UDI

Category: Dental bone matrix implant, animal-derived

Osseo Seal by Odontit S.a. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Odontit S.a.

Sources (1)

  • FDA UDI a02c58bd-dde0-41bc-a10b-fa7cb4a71b71 33 fields · synced Jun 6, 2026