AMICO CLINICAL SOLUTIONS

FDA Device Registration & Listing · Richmond Hill Ontario, CA · Registration 3007682310

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
3007682310
FEI Number
1000214453
Entity Name
AMICO CLINICAL SOLUTIONS
City/State/Country
Richmond Hill Ontario, CA
Establishment Address
122 East Beaver Creek Rd, Richmond Hill Ontario L4B 1G6, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Amico Clinical Solutions (Owner Number: 10031255)
Owner / Operator Contact Address
122 East Beaver Creek Rd, Richmond Hill, CA-ON L4B 1G6, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Spectra, Saturn and V-Series Pendant-Boom Pearl 130 & 160 MC patient lift Amico iCE LED Light

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQO Table, Operating-Room, Ac-Powered General, Plastic Surgery Class 1 878.4960 2010-02-10
FSY Light, Surgical, Ceiling Mounted General, Plastic Surgery Class 2 878.4580 2010-05-17
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2010-02-19
FSY Light, Surgical, Ceiling Mounted General, Plastic Surgery Class 2 878.4580 2013-12-05

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 Clinical Solutions
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
K780666 Castle Co. DAYSTAR SELECTRA & SELECTRA/ORBITER 1978-04-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0036-2024 Getinge Usa Sales Inc 1
Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment. Model Number: 7200.01F2
Z-0028-2016 Resource Optimization & Innovation Llc 2
regard Item Number: 800091, Sterile, LD0692 - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical procedure
Z-0029-2016 Resource Optimization & Innovation Llc 2
regard Item Number: 800401, Sterile, GS0470 - Lap Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical procedure
Z-0030-2016 Resource Optimization & Innovation Llc 2
regard Item Number: 800407, Sterile, OR0476 - Ortho Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROI, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical procedure
Z-0031-2016 Resource Optimization & Innovation Llc 2
regard Item Number: 800408, Sterile, LD0477 - C-Section Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROI, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical procedure

Similar Registrations

Registration Number Establishment Name Location
3031025858 HERR ENTERPRISES INC Jasper, AL, US
3006800085 IHB OPERATIONS Zwolle Overijssel, NL
3044829820 UNITED SURGICAL INDUSTRIES SAHIBABAD Uttar Pradesh, IN
3007836437 HOSMED INC. Doral, FL, US
3006105501 DRASHTI MEDICAL SOLUTIONS, LLC Rockledge, FL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007682310. Last updated year: 2026. Please use registration number 3007682310 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.