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Expose

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
Expose FDA UDI
Generic Name
Dental caries detecting stain FDA UDI
Device Name
Expose Refill Red Fine FDA UDI
Model / Reference
310333 FDA UDI
Description
Expose Refill Red Fine FDA UDI

Identifiers

Primary DI / UDI-DI
00817051022369 FDA UDI
510(k) Number
K963927 FDA UDI
FDA Product Code
LFC FDA UDI
GMDN Term
Dental caries detecting stain FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1740 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental caries detecting stain

Expose by Centrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental caries detecting stain.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI dc9ae2b6-ef42-490a-b0e2-8d8f7a28f220 34 fields · synced May 30, 2026