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Cm Loc®

FDA UDI

Class I (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name
CM LOC® FDA UDI
Generic Name
Dental precision attachment fitting/adjustment tool FDA UDI
Device Name
CM LOC® Housing Extractor FDA UDI
Model / Reference
07000217 FDA UDI
Description
CM LOC® Housing Extractor FDA UDI

Identifiers

Catalog Number
07000217 FDA UDI
Primary DI / UDI-DI
07640166511359 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental precision attachment fitting/adjustment tool FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental precision attachment fitting/adjustment tool

Cm Loc® by Cendres+Métaux SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental precision attachment fitting/adjustment tool.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cendres+Métaux SA

Sources (1)

  • FDA UDI c265e173-b22b-493a-8745-b28bb64e8d40 36 fields · synced May 31, 2026