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Applied BioPhotonics Phototherapy System

FDA UDI

Class II (US FDA UDI)

by Applied Biophotonics , Ltd.

Identity

Trade Name
Applied BioPhotonics Phototherapy System FDA UDI
Generic Name
Red-light phototherapy unit, professional FDA UDI
Model / Reference
ABPT1003 FDA UDI

Identifiers

Primary DI / UDI-DI
04719873240012 FDA UDI
510(k) Number
K142256 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Red-light phototherapy unit, professional 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Red-light phototherapy unit, professionalMusculoskeletal infrared phototherapy unit, non-wearable

Applied BioPhotonics Phototherapy System by Applied Biophotonics , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal infrared phototherapy unit, non-wearable.

Cleared under the same submission

K142256 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Applied Biophotonics , Ltd.

Sources (1)

  • FDA UDI 460e05b2-1d4e-472d-b16d-03b84d78c86a 34 fields · synced May 30, 2026