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Poly Pro

FDA UDI

Class II (US FDA UDI)

by Medtek Lighting Corp

Identity

Trade Name
Poly Pro FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Device Name
LED Light Therapy Device. Uses 1820 LEDs at 633nm to treat facial wrinkles. Available for use in Salons, Spas, Med Spas, Dermatology. FDA UDI
Model / Reference
Poly Pro Rejuv FDA UDI
Description
LED Light Therapy Device. Uses 1820 LEDs at 633nm to treat facial wrinkles. Available for use in Salons, Spas, Med Spas, Dermatology. FDA UDI

Identifiers

Primary DI / UDI-DI
B3437000A2 FDA UDI
510(k) Number
K180875 FDA UDI
FDA Product Code
OHS 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 Conditional FDA UDI

Category: Blue/red/infrared phototherapy lamp

Poly Pro 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 d4d78814-acbc-4d09-a784-bab4c4d8990c 35 fields · synced Jun 1, 2026