← Back to catalogue

Flex Tab

FDA UDI

Class I (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Flex Tab FDA UDI
Generic Name
Interproximal/occlusal dental gauge, single-use FDA UDI
Device Name
Flexible Clearance Tabs (Green) FDA UDI
Model / Reference
004-007 FDA UDI
Description
Flexible Clearance Tabs (Green) FDA UDI

Identifiers

Primary DI / UDI-DI
10841396117302 FDA UDI
FDA Product Code
EFH FDA UDI
GMDN Term
Interproximal/occlusal dental gauge, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6140 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

No

FDA UDI

Dimensions & Sizes

Size
Height — 1.5 Millimeter FDA UDI

Category: Interproximal/occlusal dental gauge, single-use

Flex Tab by Kerr Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Interproximal/occlusal dental gauge, single-use.

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

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI b7e63fd6-e1bc-4b97-9f7c-a6df28eadc23 36 fields · synced Jun 8, 2026