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Cala kIQ

FDA UDI

Class II (US FDA UDI)

by Cala Health, Inc.

Identity

Trade Name
Cala kIQ FDA UDI
Generic Name
Tremor-suppression transcutaneous electrical stimulation wristband FDA UDI
Device Name
Stimulator FDA UDI
Model / Reference
TLA-3268 FDA UDI
Description
Stimulator FDA UDI

Identifiers

Primary DI / UDI-DI
00851749007412 FDA UDI
FDA Product Code
QBC FDA UDI
GMDN Term
Tremor-suppression transcutaneous electrical stimulation wristband FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5897 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

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: Tremor-suppression transcutaneous electrical stimulation wristband

Cala kIQ by Cala Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tremor-suppression transcutaneous electrical stimulation wristband.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cala Health, Inc.

Sources (1)

  • FDA UDI 921ed459-4b92-4165-a80a-189fa2f6c58c 35 fields · synced Jun 8, 2026