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Kontour™ Adapt

FDA UDI

Class II (US FDA UDI)

by Implant Direct Sybron Manufacturing Llc

Identity

Trade Name
Kontour™ Adapt FDA UDI
Generic Name
Collagen dental regeneration membrane FDA UDI
Device Name
Kontour™ Adapt Resorbable Collagen Membrane - 30mm x 40mm FDA UDI
Model / Reference
KRMA3040 FDA UDI
Description
Kontour™ Adapt Resorbable Collagen Membrane - 30mm x 40mm FDA UDI

Identifiers

Catalog Number
KRMA3040 FDA UDI
Primary DI / UDI-DI
10841307130536 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

Kontour™ Adapt by Implant Direct Sybron Manufacturing Llc — 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 e94850fc-d8c2-48b2-9157-c11031b20588 37 fields · synced Jun 1, 2026