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Bosworth Ultra Trim

FDA UDI

Class II (US FDA UDI)

by Harry J. Bosworth Co.

Identity

Trade Name
Bosworth Ultra Trim FDA UDI
Generic Name
Temporary dental crown/bridge resin FDA UDI
Device Name
Bis-Acryl C&B Cartridge, A1 FDA UDI
Model / Reference
0921806 FDA UDI
Description
Bis-Acryl C&B Cartridge, A1 FDA UDI

Identifiers

Catalog Number
0921806 FDA UDI
Primary DI / UDI-DI
H66809218061 FDA UDI
FDA Product Code
EBG FDA UDI
GMDN Term
Temporary dental crown/bridge resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 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

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

No

FDA UDI

Dimensions & Sizes

Size
Weight — 76 Gram FDA UDI
Total Volume — 50 Milliliter FDA UDI

Bosworth Ultra Trim by Harry J. Bosworth Co. — Class II — 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 11a7892c-3591-49e2-ac6b-ccb237a2fffd 38 fields · synced Jun 6, 2026