Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014730563

FEI Number

3014730563

Entity Name

ROCOTO LTD.

City/State/Country

Raanana Central, IL

Establishment Address

Zarhin 26, Raanana Central 4366250, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Rocoto Ltd. (Owner Number: 10087616)

Owner / Operator Contact Address

Zarhin 26, Raanana, IL-M 4366250, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MD 62 System Receiver MD 11 System Receiver MD 62 System Transmitter MD 11 System Transmitter MD 52 System Transmitter MD 52 System Receiver HM11 Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OUG	Medical Device Data System	General Hospital	Class 1	880.6310	2023-03-21
HPP	Headlamp, Operating, Battery-Operated	Ophthalmic	Class 1	886.4335	2025-03-26

Official Correspondent

Guillermo Dyk

US Agent Details

Rafael Agiv Email: rafi.agiv@rocotosolutions.com Phone: (949) 6897863

Related Public Records

Same Entity

Rocoto Ltd.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3035371773	Rocoto Inc.	Irvine, CA, US
3006993514	AboCom Systems, Inc.	Zhunan Township Miaoli, TW

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3002725312	AMERICAN PORTWELL TECHNOLOGY, INC.	Fremont, CA, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014730563. Last updated year: 2026. Please use registration number 3014730563 when referencing this establishment in official correspondence.