TAVTECH, LTD.

FDA Device Registration & Listing · YEHUD Central, IL · Registration 9615063

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
9615063
FEI Number
3003821398
Entity Name
TAVTECH, LTD.
City/State/Country
YEHUD Central, IL
Establishment Address
40 HAATZMAUT STR., Top Rasco Bldg., YEHUD Central 5630417, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TAVTECH, LTD. (Owner Number: 9031410)
Owner / Operator Contact Address
40 HAATZMAUT STR., Top Rasco BLDG., YEHUD, IL-NOTA 5630417, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

JetPeel JetPro TOGO JetPro JetPro Duo Jetox

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2015-02-26
FQH Lavage, Jet General Hospital Class 2 880.5475 1999-08-04

Official Correspondent

No official correspondent registered.

US Agent Details

Naphtali Deutsch Business: A. STEIN - REGULATORY AFFAIRS CONSULTING LTD. Email: ahava@asteinrac.com Phone: (888) 4433867

Related Public Records

Same Entity

TAVTECH, 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
K213616 Becton, Dickinson and Company BD Surgiphor Antimicrobial Irrigation System 2022-03-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9615063. Last updated year: 2026. Please use registration number 9615063 when referencing this establishment in official correspondence.
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