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POLY Go

FDA UDI

Class II (US FDA UDI)

by Medtek Lighting Corp

Identity

Trade Name
POLY Go FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Device Name
Hand Held LED Light Therapy Device. Uses LED to treat mild to moderate Acne. Contains rechargeable Battery FDA UDI
Model / Reference
POLY Go Clear FDA UDI
Description
Hand Held LED Light Therapy Device. Uses LED to treat mild to moderate Acne. Contains rechargeable Battery FDA UDI

Identifiers

Primary DI / UDI-DI
B3437000CA1 FDA UDI
510(k) Number
K180900 FDA UDI
FDA Product Code
OLP FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Area/Surface Area — 25 Square centimeter FDA UDI

Category: Blue/red/infrared phototherapy lamp

POLY Go by Medtek Lighting Corp — 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 7f0074f6-72c6-4b36-9a2b-489780dc5db0 35 fields · synced Jun 1, 2026