Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009079475

FEI Number

3009079475

Entity Name

Aerotel Ltd.

City/State/Country

Holon Central, IL

Establishment Address

19 Hamashbir Str., Holon Central 58117, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Aerotel USA Inc. (Owner Number: 10042270)

Owner / Operator Contact Address

608 Fifth Avenue, Suite 1010, New York, NY 10020, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MDwave DCcure MDcure

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2012-11-06

Official Correspondent

No official correspondent registered.

US Agent Details

Ted Bochi Business: Aerotel USA Inc Email: tbochi@aerotelusa.com Phone: (917) 6421806

Related Public Records

Same Entity

Aerotel USA Inc.

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 3009079475. Last updated year: 2026. Please use registration number 3009079475 when referencing this establishment in official correspondence.