Vector R&D, Inc OS45LS

by Vector R&D, Inc.

Vector R&D, Inc OS45LS is a Class I device made by Vector R&D, Inc., cleared under FDA 510(k) K152146 on 8 Dec 2015 and listed in FDA GUDID since 30 Sep 2022 (UDI-DI 00810113690971), 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	Number00810113690971 UDI-DI	Date30 Sep 2022Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK152146	Date8 Dec 2015Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00810113690971
FDA 510(k) database 510(k) number K152146

Across registries

2 registries list this device

FDA 510(k) K152146 decided 8 Dec 2015 Active
FDA GUDID UDI-DI 00810113690971 listed 30 Sep 2022 Listed

Timeline

2 dated events

8 Dec 2015 Cleared FDA 510(k) K152146
30 Sep 2022 Listed FDA GUDID 00810113690971

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Withdrawn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: OS45LS

Primary DI / UDI-DI: 00810113690971
510(k) Number: K152146
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)