Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020246591

FEI Number

3020246591

Entity Name

Precision Technology Services Ltd

City/State/Country

Cambridge Ontario, CA

Establishment Address

7-38 Cowansview Road, Cambridge Ontario N1R 7N3, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

PRECISION TECHNOLOGY SERVICES, LTD. (Owner Number: 9052199)

Owner / Operator Contact Address

7-38 Cowansview Rd., Cambridge, CA-ON N1R 7N3, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Rigid Gas Permeable Contact Lens PC-IV Daily Wear ICD Flexfit Keratoconus Bi-Aspheric (KBA) Smartlens Medmont E300 Corneal Topographer Smartlens Smartlens ICD Flexfit ICD Flexfit Smartlens Moonlens Flex Moonlens OTZ Triad Apex Daily Wear TriCurve Medmont Meridia Advanced Topographer Classic Topographer Corneal AC-Powered Medmont corneal topographer Smartlens ICD Flexfit Medmont Automated Perimeter M700 USB CR Medmont Automated Perimeter M700 USB C Medmont Automated Perimeter M730 USB Medmont Automated Perimeter M730 Medmont Automated Perimeter M700 USB

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2007-10-24
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2025-01-19
HLQ	Keratoscope, Ac-Powered	Ophthalmic	Class 1	886.1350	2002-07-19
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-10-22
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-10-22
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-10-22
MUW	Lens, Contact (Orthokeratology)	Ophthalmic	Class 2	886.5916	2022-10-22
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-10-22
MMQ	Topographer, Corneal, Ac-Powered	Ophthalmic	Class 1	886.1350	2019-12-18
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-10-22
HPT	Perimeter, Automatic, Ac-Powered	Ophthalmic	Class 1	886.1605	2002-07-19

Official Correspondent

Kevin Walls

US Agent Details

Kevin Walls Business: Regulatory Insight, Inc. Email: kevin@reginsight.com Phone: (720) 9625412

Related Public Records

Same Entity

PRECISION TECHNOLOGY SERVICES, LTD.

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
K963512	Benz Research and Development Corp.	BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL	1997-07-31

Similar Registrations

Registration Number	Establishment Name	Location
3032010300	TIANJIN MASTERVISION TECHNOLOGY CO., LTD.	Wuqing District Tianjin, CN
3005994941	SOLOTICA INDUSTRIA E COMERCIO LTDA	Sao Paulo, BR
3010607087	Menicon Nect Co., Ltd., Gujo Plant	Gujo Gifu, JP
1835957	ART OPTICAL CONTACT LENS, INC.	Walker, MI, US
3025308027	BIOLENS LAB	Mohammedia Mohammadia, MA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020246591. Last updated year: 2026. Please use registration number 3020246591 when referencing this establishment in official correspondence.