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Salvin Oramem

FDA UDI

Class II (US FDA UDI)

by Salvin Dental Specialties, Llc

Identity

Trade Name
SALVIN ORAMEM FDA UDI
Generic Name
Dental/maxillofacial soft-tissue biomatrix implant, animal-derived FDA UDI
Device Name
Salvin OraMEM® Resorbable Collagen Membrane - 15x20mm FDA UDI
Model / Reference
ORAMEM-15X20 FDA UDI
Description
Salvin OraMEM® Resorbable Collagen Membrane - 15x20mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841336100824 FDA UDI
FDA Product Code
LYC FDA UDI
GMDN Term
Dental/maxillofacial soft-tissue biomatrix 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

No

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/maxillofacial soft-tissue biomatrix implant, animal-derived

Salvin Oramem by Salvin Dental Specialties, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/maxillofacial soft-tissue biomatrix implant, animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ccb82c2f-c5cb-46ce-8a7b-7abf018c3a49 33 fields · synced Jun 6, 2026