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Plena Flex

FDA UDI

Class II (US FDA UDI)

by Collagen Matrix, Inc.

Identity

Trade Name
PLENA FLEX FDA UDI
Generic Name
Collagen dental regeneration membrane FDA UDI
Device Name
Resorbable Collagen Membrane for Dental Surgery FDA UDI
Model / Reference
CDMPP2030 FDA UDI
Description
Resorbable Collagen Membrane for Dental Surgery FDA UDI

Identifiers

Catalog Number
CDMPP2030 FDA UDI
Primary DI / UDI-DI
00813954027043 FDA UDI
FDA Product Code
NPL FDA UDI
GMDN Term
Collagen dental regeneration membrane 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

No

FDA UDI

Category: Collagen dental regeneration membrane

Plena Flex by Collagen Matrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Collagen dental regeneration membrane.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78d35595-af27-4043-886b-efcd41c3061f 37 fields · synced Jun 8, 2026