Vector R&D, Inc ERA-NK

by Vector R&D, Inc.

Vector R&D, Inc ERA-NK is a Class I device made by Vector R&D, Inc., cleared under FDA 510(k) K051872 on 3 Oct 2005 and listed in FDA GUDID since 30 Sep 2022 (UDI-DI 00810113690582), 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	Number00810113690582 UDI-DI	Date30 Sep 2022Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK051872	Date3 Oct 2005Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00810113690582
FDA 510(k) database 510(k) number K051872

Across registries

2 registries list this device

FDA 510(k) K051872 decided 3 Oct 2005 Active
FDA GUDID UDI-DI 00810113690582 listed 30 Sep 2022 Listed

Timeline

2 dated events

3 Oct 2005 Cleared FDA 510(k) K051872
30 Sep 2022 Listed FDA GUDID 00810113690582

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Withdrawn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 power tool handpiece motorless component
Model / Ref / Catalog: ERA-NK

Primary DI / UDI-DI: 00810113690582
510(k) Number: K051872
FDA product code: EFB
GMDN term: Dental power tool handpiece motorless component

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

MRI safety: MR Unsafe

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Properties

Other properties (15, all answered No)