i-Fix Partnership & distribution

Bring us the case, or the territory.

Enquiries are answered by the manufacturing team in India — the same people who machine, inspect and pack the implants.

02 Scope of supply

The implant, the prosthetic components
and the surgical kit are engineered as one system.

8 implant series spanning bone-level, one-piece, compressive and zygomatic applications, together with the PSI patient-specific line and an in-house digital dental laboratory.

03 Doctors and distributors

Let's work together.

CE · NB 2803 MDR transition confirmed, 30 May 2024
50,000 sq ft Single-site manufacturing floor
ISO 13485:2016 Quality system, certified to 01/09/2027

For doctors

Clinical and technical questions go to the team that designs and manufactures the implant system.

  • Technical support from the engineers who hold the drawing for the part
  • Diameter- and length-matched drilling protocols published per series
  • Catalogs, IFUs and case-specific documentation on request

For distributors

An export-ready facility in India and one point of contact for regional distribution and private-label discussions.

  • Full quality-system and conformity documentation for market onboarding
  • Territory, volume and private-label terms discussed with the manufacturing team
  • One contact for pricing, supply and regional exclusivity questions

04 Distributor onboarding

Distributor onboarding.

The agreement is signed with Kamal Medtech Private Limited at the manufacturing plant, and the same desk answers the technical and regulatory questions that follow it.

Territory and volume terms

Regional exclusivity, order volumes and pricing, agreed per territory.

Private-label enquiries

Private-label and co-branding requests are quoted case by case. Send the specification and volumes for current terms.

The document pack

EN ISO 13485:2016 certificate, EU MDR transition confirmation, product catalogs, the IFU set and the Form MD-9 manufacturing licence.

05 Frequently asked

Before you reach out.

The manufacturing team at the manufacturing facility, which machines, inspects and packs the implants. Pricing, territory and documentation questions are all answered from there.

The EN ISO 13485:2016 certificate, the EU MDR transition confirmation (reference IN_014458_2024_01, Notified Body 2803), the product catalogs, the IFU set and the Form MD-9 manufacturing licence.

Technical support on a case, the diameter- and length-matched drilling protocol for a series, and the catalog or IFU for any implant in the portfolio.

At Kamal Medtech, India — a 50,000 sq ft facility operating under EN ISO 13485:2016.

Tell us the region, or the case.

info@ifiximplant.com and +91 99710 16943 reach the same desk as the form.

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