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ViMove+

FDA UDI

Class I (US FDA UDI)

by Dorsavi Ltd

Identity

Trade Name
ViMove+ FDA UDI
Generic Name
Psychophysiological biofeedback system FDA UDI
Device Name
ViMove+ is a wireless medical device that measures, records, and reports movements and muscle activity of the lower back / lumbar spine. The system also measures range of motion in the sagittal and coronal anatomical planes. FDA UDI
Model / Reference
000VMPLU0 FDA UDI
Description
ViMove+ is a wireless medical device that measures, records, and reports movements and muscle activity of the lower back / lumbar spine. The system also measures range of motion in the sagittal and coronal anatomical planes. FDA UDI

Identifiers

Catalog Number
VMPLU FDA UDI
Primary DI / UDI-DI
B758000VMPLU0 FDA UDI
510(k) Number
K163150 FDA UDI
FDA Product Code
KQX FDA UDI
HCC FDA UDI
IKN FDA UDI
GMDN Term
Psychophysiological biofeedback system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1500 FDA UDI
882.5050 FDA UDI
890.1375 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Psychophysiological biofeedback system

ViMove+ by Dorsavi Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Psychophysiological biofeedback system.

Cleared under the same submission

K163150 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dorsavi Ltd

Sources (1)

  • FDA UDI 83133e4a-9c17-4b4d-be72-5e21ed8b734e 36 fields · synced May 30, 2026