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OsseoSeal

FDA UDI

Class II (US FDA UDI)

by HYUNDAI BIOLAND Co., Ltd.

Identity

Trade Name
OsseoSeal FDA UDI
Generic Name
Collagen dental regeneration membrane FDA UDI
Device Name
Resorbable Collagen Membrane FDA UDI
Model / Reference
OS2030 FDA UDI
Description
Resorbable Collagen Membrane FDA UDI

Identifiers

Primary DI / UDI-DI
08800048502243 FDA UDI
510(k) Number
K200623 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

Dimensions & Sizes

Size
Length — 30 Millimeter FDA UDI
Width — 20 Millimeter FDA UDI

Category: Collagen dental regeneration membrane

OsseoSeal by HYUNDAI BIOLAND Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Collagen dental regeneration membrane.

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 0bdf785c-b89c-4447-b194-977f85a72189 35 fields · synced Jun 8, 2026