MyndMove Electrode Cable Brown

by Myndtec, Inc. 2 variants

MyndMove Electrode Cable Brown (900125) is a Class II device made by Myndtec, Inc., cleared under FDA 510(k) K170564 on 30 Aug 2017 and listed in FDA GUDID since 11 Dec 2019 (UDI-DI 00692520001256), 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	Number00692520001256 UDI-DI	Date11 Dec 2019Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK170564	Date30 Aug 2017Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00692520001256
FDA 510(k) database 510(k) number K170564

Across registries

2 registries list this device

FDA 510(k) K170564 decided 30 Aug 2017 Active
FDA GUDID UDI-DI 00692520001256 listed 11 Dec 2019 Listed

Timeline

2 dated events

30 Aug 2017 Cleared FDA 510(k) K170564
11 Dec 2019 Listed FDA GUDID 00692520001256

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: MyndMove
Generic name: Neuromuscular transmission electrode/sensor lead
Model / Ref / Catalog: MyndMove Electrode Cable Brown, 900125

Primary DI / UDI-DI: 00692520001256
510(k) Number: K170564
FDA product code: IPF, GZI
GMDN term: Neuromuscular transmission electrode/sensor lead

Device class: Class II
Regulation number: 890.5850, 882.5810
GUDID distribution status: In Commercial Distribution

MRI safety: MR Unsafe

Other devices from Myndtec, Inc.

See all devices from Myndtec, Inc. →

Properties

Prescription use
Lot / batch number
Manufacturing date

Other properties (12, all answered No)