Vector R&D, Inc Vx10-SLK

by Vector R&D, Inc.

Vector R&D, Inc Vx10-SLK is a Class I device made by Vector R&D, Inc., cleared under FDA 510(k) K032234 on 2 Oct 2003 and listed in FDA GUDID since 30 Sep 2022 (UDI-DI 00810113690001), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

FDA submission, from GUDID

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	Number00810113690001 UDI-DI	Date30 Sep 2022Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK032234	Date2 Oct 2003Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00810113690001
FDA 510(k) database 510(k) number K032234

Across registries

2 registries list this device

FDA 510(k) K032234 decided 2 Oct 2003 Active
FDA GUDID UDI-DI 00810113690001 listed 30 Sep 2022 Listed

Timeline

2 dated events

2 Oct 2003 Cleared FDA 510(k) K032234
30 Sep 2022 Listed FDA GUDID 00810113690001

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Vector R&D, Inc
Generic name: Dental surgical power tool motorized handpiece/set, pneumatic
Model / Ref / Catalog: Vx10-SLK

Primary DI / UDI-DI: 00810113690001
510(k) Number: K032234
FDA product code: EFB
GMDN term: Dental surgical power tool motorized handpiece/set, pneumatic

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

MRI safety: MR Unsafe

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Properties

Serial number

Other properties (14, all answered No)