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mTrigger

FDA UDI

Class II (US FDA UDI)

by Mtrigger, Llc

Identity

Trade Name
mTrigger FDA UDI
Generic Name
Biomechanical function analysis/interactive rehabilitation system FDA UDI
Device Name
mTrigger Biofeedback System FDA UDI
Model / Reference
BI2612/BK2613 FDA UDI
Description
mTrigger Biofeedback System FDA UDI

Identifiers

Primary DI / UDI-DI
00863712000337 FDA UDI
FDA Product Code
HCC FDA UDI
GMDN Term
Biomechanical function analysis/interactive rehabilitation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5050 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Biomechanical function analysis/interactive rehabilitation system

mTrigger by Mtrigger, 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
Mtrigger, Llc

Sources (1)

  • FDA UDI dec66c62-a54e-4e08-8546-3a9d6e06e75f 34 fields · synced Jun 1, 2026