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Data / Medical devices / United States / Centricity Vision, Inc.

Centricity Vision, Inc.: FDA-registered device maker in Carlsbad, CA, United States, 2 510(k) clearances

Centricity Vision, Inc. is registered with the FDA (registration 3011398014) in Carlsbad, CA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 11, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3011398014
Address
1939 Palomar Oaks Way Suite A, Carlsbad, CA, United States, 92011
Owner or operator
Centricity Vision, Inc. (10055077)
Roles
Manufacturer
First device listed
April 20, 2023
Registered through
2026
Brand names listed
Zepto Precision Capsulotomy System, ZeptoLink IOL Positioning System

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 11, 2023K223763ZeptoLink IOL Positioning SystemPULSubstantially EquivalentCentricity Vision, Inc.accessdata.fda.gov
December 14, 2021K210827ZEPTO Precision Capsulotomy SystemPULSubstantially EquivalentCentricity Vision, Inc.accessdata.fda.gov

Compare with other makers

Updated April 11, 2023. 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.