Centricity Vision, Inc.

FDA Device Registration & Listing · Carlsbad, CA, US · Registration 3011398014

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3011398014
FEI Number
3011398014
Entity Name
Centricity Vision, Inc.
City/State/Country
Carlsbad, CA, US
Establishment Address
1939 Palomar Oaks Way, Suite A, Carlsbad, CA 92011, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Centricity Vision, Inc. (Owner Number: 10055077)
Owner / Operator Contact Address
1939 Palomar Oaks Way, Suite A, Carlsbad, CA 92011, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K210827
PMA Number
N/A

All Registered Proprietary Names

ZeptoLink IOL Positioning System Zepto Precision Capsulotomy System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PUL Apparatus, Cutting, Radiofrequency, Electrosurgical, Ac-Powered Ophthalmic Class 2 886.4100 2023-04-20
PUL Apparatus, Cutting, Radiofrequency, Electrosurgical, Ac-Powered Ophthalmic Class 2 886.4100 2023-05-30

Official Correspondent

Neal Hartman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Centricity Vision, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011398014. Last updated year: 2026. Please use registration number 3011398014 when referencing this establishment in official correspondence.
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