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Inspire™ Complete Provisional System Kit

FDA UDI

Class I (US FDA UDI)

by Clinician's Choice Dental Products, Inc.

Identity

Trade Name
Inspire™ Complete Provisional System Kit FDA UDI
Generic Name
Temporary dental crown/bridge resin FDA UDI
Device Name
Esthetic Provisional Composite FDA UDI
Model / Reference
152720W FDA UDI
Description
Esthetic Provisional Composite FDA UDI

Identifiers

Catalog Number
152720W FDA UDI
Primary DI / UDI-DI
07540172010986 FDA UDI
FDA Product Code
EHY FDA UDI
EID FDA UDI
EBG FDA UDI
EMA FDA UDI
ELW FDA UDI
GMDN Term
Temporary dental crown/bridge resin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6880 FDA UDI
872.4565 FDA UDI
872.3770 FDA UDI
872.3275 FDA UDI
872.3660 FDA UDI
Commercial Distribution
Not 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

Yes

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

No

FDA UDI

Inspire™ Complete Provisional System Kit by Clinician's Choice Dental Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7607c37a-1aa4-4d66-9674-489d1000193b 36 fields · synced Jun 1, 2026