I. SHERMAN

FDA Device Registration & Listing · Acre Northern, IL · Registration 3014656892

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
3014656892
FEI Number
3014656892
Entity Name
I. SHERMAN
City/State/Country
Acre Northern, IL
Establishment Address
2 Moshe Burnstein Street, South Industrial zone, Acre Northern 2410401, IL
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
I. Sherman (Owner Number: 10076323)
Owner / Operator Contact Address
2 Moshe Burnstein Street, South Industrial zone, Acre, IL-Z 2410401, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Brush, dermabrasion Powered Add Promax handpiece EndyMed Pro Skin Treatment System Add PRO MAX with handpieces: Small MAX, iFine MAX, Shaper MAX and mini-Shaper MAX Senhance Surgical System Pure by EndyMed PURE DentA

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 2025-04-21
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2022-09-29
NAY System, Surgical, Computer Controlled Instrument Gastroenterology, Urology Class 2 876.1500 2020-07-22
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2020-07-15
OUH Skin Resurfacing Rf Applicator General, Plastic Surgery Class 2 878.4400 2020-07-15

Official Correspondent

Yoram Levy

US Agent Details

Tova Rivnay Business: Qsite Email: tova@qsitemed.com Phone: (512) 5354930

Related Public Records

Same Entity

I. Sherman
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
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014656892. Last updated year: 2026. Please use registration number 3014656892 when referencing this establishment in official correspondence.
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