← Back to catalogue

Tube Lock Large Bur

FDA UDI

Class I (US FDA UDI)

by Sterngold Dental LLC

Identity

Trade Name
Tube Lock Large Bur FDA UDI
Generic Name
Sliding dental precision attachment FDA UDI
Device Name
Laboratory tool made from stainless steel. Used to remove any flash or debris left in the Large Tube Lock Female after casting. FDA UDI
Model / Reference
821055 FDA UDI
Description
Laboratory tool made from stainless steel. Used to remove any flash or debris left in the Large Tube Lock Female after casting. FDA UDI

Identifiers

Primary DI / UDI-DI
00841549116490 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Sliding dental precision attachment FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Sliding dental precision attachment

Tube Lock Large Bur by Sterngold Dental LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sliding dental precision attachment.

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 4770f119-4ace-44a2-acc2-36b802c2e9b3 34 fields · synced Jun 8, 2026