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HeliMend® Advanced

FDA UDI

Class II (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name
HeliMend® Advanced FDA UDI
Generic Name
Dental/maxillofacial soft-tissue biomatrix implant, animal-derived FDA UDI
Device Name
HeliMend® Advanced Absorbable Collagen Membrane FDA UDI
Model / Reference
62208 FDA UDI
Description
HeliMend® Advanced Absorbable Collagen Membrane FDA UDI

Identifiers

Catalog Number
62208 FDA UDI
Primary DI / UDI-DI
10381780038535 FDA UDI
510(k) Number
K992216 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

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: Dental/maxillofacial soft-tissue biomatrix implant, animal-derived

HeliMend® Advanced by Integra Lifesciences Corp. — 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eb366374-a4f8-40bd-bbcd-7cd0f00a3564 38 fields · synced May 30, 2026