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SANTA BARBARA IMAGING SYSTEMS, INC.

United States·US-MF-000007262

Last updated May 24, 2026

What SANTA BARBARA IMAGING SYSTEMS, INC. makes

Santa Barbara Imaging Systems, Inc. manufactures endoscopic imaging systems, including reusable rigid optical arthroscopes and laparoscopes, endoscopic video cameras, and associated components like video processing units, remote controls, and light source adaptors. Their portfolio also includes single-use arthroscopic access cannulas and reusable instrument trays designed for surgical procedures.

The company’s devices are classified under Class I and Class II regulations, with listings in the EU’s eudamed database and the FDA’s Unique Device Identifier (UDI) system. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Santa Barbara Imaging Systems, Inc. primarily manufacture?

Santa Barbara Imaging Systems, Inc. specializes in endoscopic imaging systems and related components. Their portfolio includes reusable rigid optical arthroscopes and laparoscopes, endoscopic video cameras, video image processing units, remote controls, and light source adaptors. They also produce single-use arthroscopic access cannulas and reusable instrument trays, all designed to support surgical procedures.

Where is Santa Barbara Imaging Systems, Inc. based?

The company is headquartered in the United States. While the exact location isn’t specified, its regulatory listings confirm its operational base within the country.

Which regulatory databases list devices manufactured by Santa Barbara Imaging Systems, Inc.?

Devices from Santa Barbara Imaging Systems, Inc. are listed in the EU’s eudamed database and the FDA’s Unique Device Identifier (UDI) system. These registries help track and verify the devices’ compliance and availability in their respective markets.

How are the devices produced by Santa Barbara Imaging Systems, Inc. classified under medical device regulations?

The company’s devices fall under Class I and Class II classifications. Class I devices generally pose minimal risk and may require fewer regulatory controls, while Class II devices involve moderate risk and typically require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and scrutiny each device undergoes.

Why are some of Santa Barbara Imaging Systems, Inc.’s devices listed in both eudamed and the FDA’s UDI system?

The presence of devices in both eudamed and the FDA’s UDI system reflects their market reach. The EU’s eudamed database is used for devices placed on the European market, while the FDA’s UDI system tracks devices in the United States. Listing in both indicates the company’s devices are authorized for use in both regulatory jurisdictions.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
340 Storke Rd., Goleta, United States
LinkedIn
—
Facebook
—
Phone
805-770-2110
PRRC Contact
James Candy
EUDAMED SRN
US-MF-000007262
FDA FEI Number
—
DUNS Number
065016344

Catalogue (153)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
Pixa 85-10-6430-U
FDA UDI
Class IIActive
Zeos 84-14-2800
FDA UDI
Class IIActive
Zeos 84-24-4111
FDA UDI
Class IActive
Zeos 84-24-4022
FDA UDI
Class IActive
Zeos 84-10-5130
FDA UDI
Class IIActive
Zeos 84-24-1922
FDA UDI
Class IActive
Zeos 84-20-5002
FDA UDI
Class IIActive
Zeos 84-10-4101
FDA UDI
Class IIActive
Zeos 84-24-4020
FDA UDI
Class IActive
Trinity 81-10-2210
FDA UDI
Class IIActive
Zeos 84-10-5110
FDA UDI
Class IIActive
Zeos 84-10-4410
FDA UDI
Class IIActive
Imaging (ZEOS) 84-10-2130
FDA UDI
Class IIActive
Zeos 84-10-2210
FDA UDI
Class IIActive
Imaging (ZEOS) 84-10-4010
FDA UDI
Class IIActive
Pixa 85-10-6431
FDA UDI
Class IIActive
Zeos 84-10-1500T
FDA UDI
Class IIActive
Zeos 84-14-5548
FDA UDI
Class IIActive
Omni 83-20-5003
FDA UDI
Class IIActive
Pixa 85-10-6530
FDA UDI
Class IIActive
Zeos 84-24-4110
FDA UDI
Class IActive
Imaging (ZEOS) 84-20-50037
FDA UDI
Class IActive
Pixa 85-10-4120
FDA UDI
Class IIActive
Pixa 85-10-5101
FDA UDI
Class IIActive
Zeos 84-24-2722
FDA UDI
Class IActive
Trinity 81-10-2010
FDA UDI
Class IIActive
Zeos 84-14-2700
FDA UDI
Class IIActive
Zeos 84-20-5003
FDA UDI
Class IIActive
Zeos 84-24-4042
FDA UDI
Class IActive
Imaging (ZEOS) 84-10-4100
FDA UDI
Class IIActive
Pixa 85-10-4130
FDA UDI
Class IIActive
Zeos 84-24-2720
FDA UDI
Class IActive
Imaging (ZEOS) 84-10-4120
FDA UDI
Class IIActive
Imaging (ZEOS) 84-10-2010
FDA UDI
Class IIActive
Zeos 84-14-5547
FDA UDI
Class IIActive
Pixa 85-10-2010
FDA UDI
Class IIActive
Zeos 84-14-1000
FDA UDI
Class IIActive
Zeos 84-10-4320
FDA UDI
Class IIActive
Zeos 84-10-5101
FDA UDI
Class IIActive
Omni 83-10-4010
FDA UDI
Class IIActive
Imaging (ZEOS) 84-10-4110
FDA UDI
Class IIActive
Pixa 85-10-4110
FDA UDI
Class IIActive
Zeos 84-14-4230
FDA UDI
Class IIActive
Pixa 85-10-6431-U
FDA UDI
Class IIActive
Zeos 84-10-1200
FDA UDI
Class IIActive
Zeos 84-28-1150
FDA UDI
Class IActive
Omni 83-20-50032
FDA UDI
Class IActive
Pixa 85-10-5121
FDA UDI
Class IIActive
Omni 83-10-1500T
FDA UDI
Class IIActive
Zeos 84-10-4330
FDA UDI
Class IIActive

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