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FlexiStrips Narrow Coarse/Medium

FDA UDI

Class I (US FDA UDI)

by Cosmedent, Inc.

Identity

Trade Name
FlexiStrips Narrow Coarse/Medium FDA UDI
Generic Name
Dental abrasive disk, single-use FDA UDI
Model / Reference
501CMN FDA UDI

Identifiers

Primary DI / UDI-DI
D779501CMN1 FDA UDI
FDA Product Code
EHM FDA UDI
GMDN Term
Dental abrasive disk, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental abrasive disk, single-use

FlexiStrips Narrow Coarse/Medium by Cosmedent, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental abrasive disk, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cosmedent, Inc.

Sources (1)

  • FDA UDI 79f179c6-63db-4830-bbeb-7d5e870eb7bb 32 fields · synced Jun 1, 2026