AMICO LIGHTS CORPORATION

FDA Device Registration & Listing · Richmond Hill Ontario, CA · Registration 3009791213

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009791213
FEI Number
3009791213
Entity Name
AMICO LIGHTS CORPORATION
City/State/Country
Richmond Hill Ontario, CA
Establishment Address
122 East Beaver Creek Road, Richmond Hill Ontario L4B 4V1, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Amico Lights Corporation (Owner Number: 10046356)
Owner / Operator Contact Address
122 East Beaver Creek Road, Richmond Hill, CA-ON L4B 4V1, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Multiple SCA Mira Examination Light Multiple SKY Multiple GAMMA Multiple CLARITY Multiple MIRA Multiple LUNAR Multiple SLM Multiple VEGA Multiple SOL Multiple SDM Multiple NOVA Multiple CLR Multiple ECLIPSE Multiple MAGNA Multiple LINEA Multiple SDE Multiple DWN Multiple SURG Multiple LVC Multiple MASTER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZF Device, Medical Examination, Ac Powered General Hospital Class 1 880.6320 2022-05-20

Official Correspondent

No official correspondent registered.

US Agent Details

Jon Ward Business: AJW Technology Consultants, Inc. Email: usagent@ajwtech.com Phone: (813) 6452855

Related Public Records

Same Entity

Amico Lights Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K851742 Burton Medical Products Corp. MEDICAL EXAMINATION LIGHTS 1985-05-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009791213. Last updated year: 2026. Please use registration number 3009791213 when referencing this establishment in official correspondence.
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