Cellulize

Cellulize, Green Light (532nm)

Registry build 21.09.26
6manufacturers in China registered for this device type
1catalogue number
3recalls on this code

Who Else Makes It

Concentrated in Guangdong (3), Beijing (2), Henan (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OLI
Manufacturer City Province Registered as Device types
Beijing Syntech Laser Co., Ltd. Beijing Beijing Contract manufacturer 5
Beijing Spiritlaser Science & Technology Co., Ltd. Beijing Beijing Contract manufacturer 21
Shenzhen Kaiyan Medical Equipment Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
Zhengzhou PZ Laser Slim Technology Co., Ltd. Zhengzhou Henan Manufacturer 6
Shenzhen Light Tree Ventures Medical Technology Co., Ltd. Shenzhen Guangdong Exporter 6
Shenzhen Suyzeko Limited Shenzhen Guangdong Contract manufacturer 4

Record

Regulatory record for Cellulize
Listed by Photonica USA LLC, United States
FDA product code OLI
Device type Fat Reducing Low Level Laser
Device class Class 2
Regulation 21 CFR 878.5400
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K180338
Record published 2020-01-17
Record revised 2026-07-21 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only

Catalogue Numbers

Catalogue numbers for Cellulize
Catalogue number Size Status
60002 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Led Light Phototherapy Bed Shenzhen Suyzeko Limited 2
Erchonia Zerona VZ8 Erchonia Corporation 1
Emerald Erchonia Corporation 1
Zerona 2.0 Erchonia Corporation 1
Verju Erchonia Corporation 1
Erchonia CLX Erchonia Corporation 1
Zerona Z6 Erchonia Corporation 1
Photonica Professional Photonica USA LLC 1
UltraSlim Digital Photonica USA LLC 1
R11 Air KBL GmbH 1
Erchonia Zerona Z-Bed Erchonia Corporation 1
Zerona AD Erchonia Corporation 1

Showing 12 of 13. All products under Fat Reducing Low Level Laser

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. 3 are recorded with the root cause “No Marketing Application”: the device was distributed without the premarket submission its class requires, a compliance finding rather than a defect. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2014-05-06 Class II No Marketing Application Marketing without marketing clearance or approval. 235 Total 2015-06-24
2014-05-06 Class II No Marketing Application Marketing without marketing clearance or approval. 235 Total 2015-06-24
2014-05-06 Class II No Marketing Application Marketing without marketing clearance or approval. 235 Total 2015-06-24

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer