← Back to catalogue

OUSIA bioADAPT

FDA UDI

Class II (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
OUSIA bioADAPT FDA UDI
Generic Name
Collagen dental regeneration membrane FDA UDI
Device Name
OUSIA bioADAPT 20x30MM RESORBABLE DENTAL MEMBRANE FDA UDI
Model / Reference
OUSB2S FDA UDI
Description
OUSIA bioADAPT 20x30MM RESORBABLE DENTAL MEMBRANE FDA UDI

Identifiers

Catalog Number
OUSB2 FDA UDI
Primary DI / UDI-DI
00614950008209 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

OUSIA bioADAPT by Ace Surgical Supply Co., 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d71c4064-8226-4df0-b9f5-42f4fac34ed6 36 fields · synced May 30, 2026