← Back to catalogue

Bosworth Original Truliner

FDA UDI

Class II (US FDA UDI)

by Harry J. Bosworth Co.

Identity

Trade Name
Bosworth Original Truliner FDA UDI
Generic Name
Denture reliner, hard FDA UDI
Device Name
1 lb bulk Orig Truliner PMMA P&L Kit Pink FDA UDI
Model / Reference
0921951 FDA UDI
Description
1 lb bulk Orig Truliner PMMA P&L Kit Pink FDA UDI

Identifiers

Catalog Number
0921951 FDA UDI
Primary DI / UDI-DI
H66809219511 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture reliner, hard 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

Yes

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

Category: Denture reliner, hard

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

Similar devices

Also classified as Denture reliner, hard.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1c777e6d-d984-4baa-a111-58b138d6c4ef 36 fields · synced Jun 8, 2026