Maxso SL3019

by Beyes Dental Canada Inc 2 variants

Maxso SL3019 (X92) is a Class I device made by Beyes Dental Canada Inc, listed in FDA GUDID since 11 May 2023 (UDI-DI 00990010301900), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00990010301900 UDI-DI	Date11 May 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00990010301900

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Maxso
Generic name: Dental power tool handpiece motorless component
Model / Ref / Catalog: SL3019, X92

Primary DI / UDI-DI: 00990010301900
FDA product code: EGS
GMDN term: Dental power tool handpiece motorless component

Device class: Class I
Regulation number: 872.4200
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization
MRI safety: MR Safe

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Properties

Sterilise before use
Prescription use
Lot / batch number
Serial number
Manufacturing date

Other properties (10, all answered No)