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Beoka

FDA UDI

Class II (US FDA UDI)

by Sichuan Qianli-Beoka Medical Technology, Inc.

Identity

Trade Name
BEOKA FDA UDI
Generic Name
Wearable electric massager FDA UDI
Device Name
The Air Compression Massager is an air pressure massager intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. FDA UDI
Model / Reference
ACM-A1/Black S (Luxury version) FDA UDI
Description
The Air Compression Massager is an air pressure massager intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. FDA UDI

Identifiers

Primary DI / UDI-DI
06950735811607 FDA UDI
510(k) Number
K241446 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Wearable electric massager FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5650 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wearable electric massager

Beoka by Sichuan Qianli-Beoka Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wearable electric massager.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c75200b2-6be1-48d9-a0b3-a1f1691a1cdc 35 fields · synced May 30, 2026