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Waya Rehab

FDA UDI

Class II (US FDA UDI)

by Wellovate Llc

Identity

Trade Name
Waya Rehab FDA UDI
Generic Name
Biomechanical function analysis/interactive rehabilitation system FDA UDI
Device Name
Waya® Rehab is a software only medical device to support rehabilitation under the guidance of a qualified healthcare professional. FDA UDI
Model / Reference
1 FDA UDI
Description
Waya® Rehab is a software only medical device to support rehabilitation under the guidance of a qualified healthcare professional. FDA UDI

Identifiers

Primary DI / UDI-DI
G741WHREHABV10 FDA UDI
FDA Product Code
ISD FDA UDI
GMDN Term
Biomechanical function analysis/interactive rehabilitation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5360 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Biomechanical function analysis/rehabilitation softwareBiomechanical function analysis/interactive rehabilitation system

Waya Rehab by Wellovate Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biomechanical function analysis/interactive rehabilitation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wellovate Llc

Sources (1)

  • FDA UDI 51428172-e414-4561-a897-91aeca50a62a 34 fields · synced Jun 6, 2026