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sgrow LED Therapy Light

FDA UDI

Class II (US FDA UDI)

by Shenzhen Sungrow LED Technology Co., LTD

Identity

Trade Name
sgrow LED Therapy Light FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Model / Reference
E2400 FDA UDI

Identifiers

Primary DI / UDI-DI
06976006410010 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blue/red/infrared phototherapy lamp

sgrow LED Therapy Light by Shenzhen Sungrow LED Technology Co., LTD — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blue/red/infrared phototherapy lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 705e9124-dbfd-4c12-9da7-c7a573b9f561 32 fields · synced Jun 1, 2026