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Cmatt

FDA UDI

Class I (US FDA UDI)

by Casco Manufacturing Solutions, Inc.

Identity

Trade Name
CMATT FDA UDI
Generic Name
Hip/knee/ankle/foot orthosis FDA UDI
Device Name
KNEE SUPPORT POSITIONING WEDGE, BETWEEN THE KNEE FDA UDI
Model / Reference
H12643 FDA UDI
Description
KNEE SUPPORT POSITIONING WEDGE, BETWEEN THE KNEE FDA UDI

Identifiers

Catalog Number
H12643 FDA UDI
Primary DI / UDI-DI
00815073029465 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Hip/knee/ankle/foot orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hip/knee/ankle/foot orthosis

Cmatt by Casco Manufacturing Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hip/knee/ankle/foot orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Casco Manufacturing Solutions, Inc.

Sources (1)

  • FDA UDI 2f05bec9-678f-484d-a6ae-f9b109db2cdb 35 fields · synced Jun 7, 2026