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Bosworth TruRepair

FDA UDI

Class II (US FDA UDI)

by Harry J. Bosworth Co.

Identity

Trade Name
Bosworth TruRepair FDA UDI
Generic Name
Denture repair kit, professional FDA UDI
Device Name
4 oz Repair Liquid FDA UDI
Model / Reference
092164 FDA UDI
Description
4 oz Repair Liquid FDA UDI

Identifiers

Catalog Number
092164 FDA UDI
Primary DI / UDI-DI
H6680921641 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture repair kit, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
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

Yes

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
Total Volume — 4 Fluid Ounce FDA UDI
Total Volume — 118 Milliliter FDA UDI

Category: Denture repair kit, professional

Bosworth TruRepair by Harry J. Bosworth Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture repair kit, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Harry J. Bosworth Co.

Sources (1)

  • FDA UDI 662f6c99-e127-42ee-9981-15a546fe911e 37 fields · synced May 30, 2026