Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017419219

FEI Number

3017419219

Entity Name

KERBER USA INC.

City/State/Country

Amherst, NY, US

Establishment Address

1576 Sweet Home Rd, Amherst, NY 14228, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Kerber USA Inc. (Owner Number: 10077850)

Owner / Operator Contact Address

1576 Sweet Home Rd., Amherst, NY 14228, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SunPowerLED Canopy SunPowerLED SuperPalm 1050 SunPowerLED Mini-Canopy SunPowerLED Palm Professional SunPowerLED Helmet -810 SunPowerLED Palm Ultimate

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILY	Lamp, Infrared, Therapeutic Heating	Physical Medicine	Class 2	890.5500	2020-10-03

Official Correspondent

Thomas Kerber

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kerber USA Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017419219. Last updated year: 2026. Please use registration number 3017419219 when referencing this establishment in official correspondence.