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Patents & Licenses

Utility Patents

Contino® & Inserter

  • US: 9,707065 B2
  • Canada: 2,769,343
  • China: ZL 2010 8 0036319.X
  • Hong Kong: 1170409
  • Israel: 217823
  • Japan: 5801804
  • Macau: J/001990
  • European Patent Office: 2459118
  • Registered: 2489118 
    • UK, Germany, France, Spain, Italy, Belgium
    • Ireland, Switzerland, Netherlands, Poland
    • Sweden, Turkey, Norway, Finland, Denmark

Contino® & System

  • US: 10,441,396
  • Canada: 3,036,320
  • China: prosecution phase
  • Hong Kong: prosecution phase
  • Israel: prosecution phase
  • Japan: 7216712
  • Macao: prosecution phase
  • Mexico: 6519
  • EU: prosecution phase

Contino® Inserter

  • US: 10,485,644
  • Canada: 3,036,324
  • European Patent Office: 3496679
  • Registered: 3496679
    • UK, Germany, France, Spain, Italy,
    • Ireland, Switzerland, Netherlands, Poland
    • Sweden, Denmark, Turkey

Design Patents

Contino®

  • US: D835784
  • Australia: 201810384
  • Canada: 179427
  • China: 201830035649.6
  • EU: 0044680718-0001
  • Hong Kong: 1800149.5
  • India: 310668
  • Israel: 61542
  • Japan: 1611487
  • Macao: D/001991
  • Mexico: 55246
  • South Korea: 30-988300

Contino® Inserter

  • US: D835273
  • Australia: 201810388
  • Brazil: BR3020180002695
  • Canada: 179428
  • China: 201830035648.1
  • EU: 004680718-0002
  • Hong Kong: 1800150.7
  • India: 301669
  • Israel: 61543
  • Japan: 1611488
  • Macao: D/001992
  • Mexico: 55265
  • South Korea: 30-987416

Contino® Gauge

  • US: D787,671
  • Brazil: BR3020160020507
  • Canada: 165,380
  • China: 201630162408.9
  • EU: 002951509-00001
  • Hong Kong: 1600849.8
  • Israel: 58530
  • Japan: 1561102
  • Macau: D/001635
  • Mexico: 51165

Trademarks

Contino®

  • Canada: TMA991,949
  • EU: 015981376

Well-being by design

  • Canada: TMA1,012,280
  • EU: 015068927

Quality Management System

ISO 13485:2016 Quality Management System (QMS) compliant with CAN, EU & US

Preparation complete for implementation of the new Medical Device Regulation.

Licenses

Canada

EU

  • Our 1,200 page technical file is virtually complete and is scheduled for submission under the Medical Device Regulation in 2024.

US

  • Pre-FDA submission completed and submission expected in 2024
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