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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
3 oz Repair Pwd, Pink FDA UDI
Model / Reference
092161 FDA UDI
Description
3 oz Repair Pwd, Pink FDA UDI

Identifiers

Catalog Number
092161 FDA UDI
Primary DI / UDI-DI
H6680921611 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
Weight — 85 Gram 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

Sources (1)

  • FDA UDI 0679501b-0069-46c5-b94e-95530b840b56 37 fields · synced May 30, 2026