← Back to catalogue

Omnipad Light Therapy, Dual 5x7 Pads

FDA UDI

Class II (US FDA UDI)

by Accelerated Care Plus Corp.

Identity

Trade Name
Omnipad Light Therapy, Dual 5x7 Pads FDA UDI
Generic Name
Musculoskeletal infrared phototherapy unit, non-wearable FDA UDI
Device Name
Infrared lamp for therapeutic healing FDA UDI
Model / Reference
76896 FDA UDI
Description
Infrared lamp for therapeutic healing FDA UDI

Identifiers

Primary DI / UDI-DI
00858703006061 FDA UDI
510(k) Number
K060191 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Musculoskeletal infrared phototherapy unit, non-wearable 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Musculoskeletal infrared phototherapy unit, non-wearable

Omnipad Light Therapy, Dual 5x7 Pads by Accelerated Care Plus Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Accelerated Care Plus Corp.

Sources (1)

  • FDA UDI c8b9e4f9-0ae1-4fe3-ad67-c3a65870bbb3 35 fields · synced Jun 8, 2026