Dia Bur DB-L42

Dia Bur DB-L42 is a Class I device made by Surgident, listed in FDA GUDID since 3 Jan 2023 (UDI-DI 08800041043149), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08800041043149 UDI-DI	Date3 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 08800041043149

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Dia Bur
Generic name: Diamond dental bur, reusable
Model / reference: DB-L42

Primary DI / UDI-DI: 08800041043149
FDA product code: NDP
GMDN term: Diamond dental bur, reusable

Device class: Class I
Regulation number: 872.3980
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (11, all answered No)