Data / Medical devices / United States / Arthrex California Technology, Incorporated
Arthrex California Technology, Incorporated: FDA-registered device maker in Santa Barbara, CA, United States, 5 510(k) clearances
Arthrex California Technology, Incorporated is registered with the FDA (registration 3006990600) in Santa Barbara, CA, United States. It lists 16 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 29, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3006990600
- Address
- 460 Ward Dr, Santa Barbara, CA, United States, 93111
- Owner or operator
- ARTHREX, INC. (1220287)
- Roles
- Contract manufacturer, Contract sterilizer, Manufacturer, Specification developer
- First device listed
- August 7, 1996
- Registered through
- 2027
- Brand names listed
- Camera Heads, Camera, Television, Surgical, Without Audio, INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT, Instrument, Special Lens, For Endoscope, Instrument, manual, surgical, general use, ORTHOPEDIC MANUAL INSTRUMENTS, SHAVER SYSTEM, VARIOUS INSTRUMENTS
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 29, 2025 | K252314 | Arthrex SutureTak Suture Anchor | MBI | Substantially Equivalent | Arthrex, Inc. | accessdata.fda.gov |
| October 16, 2025 | K251994 | Arthrex Synergy Vision Imaging System | GCJ | Substantially Equivalent | Arthrex, Inc. | accessdata.fda.gov |
| July 22, 2021 | K202582 | Arthrex SynergyID Endoscopic Imaging System | GCJ | Substantially Equivalent | Arthrex, Inc. | accessdata.fda.gov |
| February 12, 2016 | K153218 | Arthrex Synergy UHD4 System | GCJ | Substantially Equivalent | Arthrex, Inc. | accessdata.fda.gov |
| August 15, 2007 | K071756 | ENDOHUB- 1.0 ENDOSCOPIC VIDEO CAMERA SYSTEM WITH VIDEO CAPTURE | GCJ | Substantially Equivalent | Pointe Conception Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Image Processing, Radiological
- All makers of Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
- All makers of Camera, Television, Surgical, Without Audio
- All makers of Accessories, Arthroscopic
- All makers of Laparoscope, General & Plastic Surgery
- All makers of System, X-Ray, Angiographic
Updated October 29, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.