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International Distributors

If you are interested in becoming an OASIS distributor, please e-mail our International department: international@oasismedical.com

Current International OASIS Distributors

  • Argentina
  • Australia
  • Austria
  • Azerbaijan
  • Belgium
  • Brazil
  • Bulgaria
  • Canada
  • Caribbean
  • Chile
  • China - Hong Kong
  • China - Mainland
  • Colombia
  • Costa Rica
  • Croatia
  • Cyprus
  • Czech Republic
  • Denmark
  • Dominican Republic
  • Ecuador
  • Egypt
  • El Salvador
  • Finland
  • France
  • Germany
  • Greece
  • Guam
  • Guatemala
  • Hungary
  • Iceland
  • India
  • Indonesia
  • Israel
  • Italy
  • Japan
  • Jordan
  • Kuwait
  • Lebanon
  • Lithuania
  • Malaysia
  • Mexico
  • New Zealand
  • Norway
  • Oman
  • Pakistan
  • Paraguay
  • Peru
  • Philippines
  • Poland
  • Portugal
  • Puerto Rico
  • Romania
  • Russia
  • Saudi Arabia
  • Singapore
  • Slovakia
  • Slovenia
  • South Africa
  • South Korea
  • Spain
  • Sweden
  • Switzerland
  • Taiwan
  • Thailand
  • The Netherlands
  • Turkey
  • United Arab Emirates
  • United Kingdom
  • Venezuela
  • Vietnam

Registered CE Marks

  • Silicone Punctum Plugs
  • Cannulas, Needles, Cystotomes
  • HPMC Viscoelastic
  • PVA Foam Sponge Products
  • Ophthalmic I/A Sets
  • Pupillometer
  • Syringe Disc Filters
  • Eye Cautery
  • Lacrimal Instruments
  • Astigmatome
  • Microkeratome Blades
  • Extended Duration Plug
  • Disposable Bimanual Irrigation Aspiration Handpiece Set
  • Form Fit® Hydrogel Punctum Plug
  • PremierEdge® Microsurgical Knives
  • Corneal Ink Pad

European Authorized Representative:

Donawa Lifescience Consulting SRL
Piazza Albania 10
00153 Rome, Italy

The OASIS facility in Glendora, CA, is ISO 9001 certified. Our quality assurance system complies with European standard EN ISO 13485:2003.

Contact Us

To place your order by phone or speak to Customer Service directly, please contact us at:

844-820-8940 (US only)

909-305-5400 (International)

Phone Hours:
6:30am – 4:30pm PST, Monday - Friday

To report adverse events: (844) 820-8940