Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027683457

FEI Number

3027683457

Entity Name

BELKIN VISION LTD.

City/State/Country

Yavne Central, IL

Establishment Address

13 Gan Rave Blvd., Yavne Central 8122214, IL

Establishment Type(s)

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

Owner / Operator

BELKIN Vision Ltd. (Owner Number: 10091141)

Owner / Operator Contact Address

13 Gan Rave Blvd., Yavne, IL-M 8122214, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K230722

PMA Number

N/A

All Registered Proprietary Names

DSLT Treatment Pack Voyager DSLT Treatment Pack Eagle Voyager DSLT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HNC	Specula, Ophthalmic	Ophthalmic	Class 1	886.4350	2024-09-26
HQF	Laser, Ophthalmic	Ophthalmic	Class 2	886.4390	2024-07-17

Official Correspondent

No official correspondent registered.

US Agent Details

Anne-Marie Ripley Business: Regulatory Pathways Group, Inc. Email: aripley@regulatorypathways.com Phone: (661) 6458546

Related Public Records

Same Entity

BELKIN Vision Ltd.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K834060	F. & F. Koenigkramer	RELIANCE OPHTHALMIC SLIT LAMP R-083	1984-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027683457. Last updated year: 2026. Please use registration number 3027683457 when referencing this establishment in official correspondence.