Step 01
Design
In-house engineering of every implant geometry, thread profile, and connection. Validated in CAD against clinical protocols before any tooling is cut.
Surcam · Dental implant manufacturer
Designed, machined, and shipped from one facility.
Engineered in Nahariya, Israel. Direct to clinicians and labs since 2002.
2002
Founded
24 years in market
100K+
Components shipped
20+
Countries served
4
International certifications
FDA · ISO · CE · MoH
6
Major platform compatibilities
The process
How it's made
One facility. One quality system. Five steps from concept to clinic.
Step 02
Material
Titanium Grade 23 ELI bar stock, certified to ASTM F136. Every lot traceable to its source.
Step 03
Machine
Multi-axis CNC machining centers hold micron-level tolerances on every cut, running lights-out.
Step 04
Inspection
Every component is dimensionally inspected and surface-verified before it leaves the floor.
Step 05
Packaging
Sterilized, lot-coded, and sealed in medical-grade packaging for direct shipment.
What we make
Three product lines. One quality system.
Every component is designed, machined, and inspected in the same facility, on the same quality system.
Implants
Bone level, tissue level, cortical, compressive, pterygoid, and zygomatic. Internal hex and conical connection systems.
View catalog
Prosthetic components
Abutments, multi-unit, CAD/CAM Ti-bases, healing caps, transfers, casting abutments, and overdenture attachments.
View catalog
Surgical tools
Implant drills, drivers, wrenches, prosthetic screws, surgical kits and trays, extraction and maintenance tools.
View catalogFit & stability
Designed to manufacturer specifications for clean seating and predictable osseointegration.
Compatibility
Cross-compatible with Alpha-Bio, BioHorizons, Implant Direct, MIS, Nobel Biocare, and Zimmer Biomet platforms.
Workflow support
Digital library, CAD files, and scan bodies available for chairside and lab workflows.
Direct economics
Direct from manufacturer. No distributors, no markup. Free shipping over $350.
Compliance
Four registrations. One file you can request.
Surcam is registered as a medical-device manufacturer in the US, EU, and Israel — and operates under an ISO 13485:2016 quality system audited annually by an accredited certification body.
For procurement reviewers:
All certificates are available as PDFs. K-numbers, Notified Body IDs, and registration numbers can be verified independently through each authority's public database.
United States
FDA 510(k)
Cleared for marketing in the United States. Substantial equivalence to predicate devices established under section 510(k) of the Food, Drug, and Cosmetic Act.
K-number: K242217
International
ISO 13485:2016
Quality management system for the design and manufacture of medical devices. Independently audited annually by an accredited certification body.
Registration No: D1440500006
European Union
CE Marked
Conformity assessment completed under EU Medical Device Regulation (MDR) 2017/745. Audited by Notified Body.
Registration No: D1440500005
Israel
Israel MoH (AMAR)
Registered with the Israeli Ministry of Health's medical device division for manufacturing and marketing.
Registration: 28010004
Why direct
No distributors. No markup. We make it ourselves.
When you order from Surcam, you're buying from the people who designed and machined the part. The same facility ships it. The same engineers answer your questions.
Let's talk
Three ways to start working with Surcam
Browse the catalog, download our product reference, or send a question. We answer within one business day.
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Full product reference with platform compatibility, dimensions, and ordering codes.
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