Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011977270

FEI Number

3011977270

Entity Name

OVITZ CORPORATION

City/State/Country

Rochester, NY, US

Establishment Address

260 East Main Street, suite 6103, Rochester, NY 14604, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Ovitz Corporation (Owner Number: 10050987)

Owner / Operator Contact Address

260 East Main Street, suite 6103, Rochester, NY 14604, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

xwave p10

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NCF	Aberrometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2019-12-31
HKO	Refractometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2016-01-23

Official Correspondent

Joung Yoon Kim

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ovitz Corporation

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011977270. Last updated year: 2026. Please use registration number 3011977270 when referencing this establishment in official correspondence.