TWM- TSADIK WEISER MEDICAL LTD

FDA Device Registration & Listing · Otniel Southern, IL · Registration 3038185753

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
3038185753
FEI Number
3038185753
Entity Name
TWM- TSADIK WEISER MEDICAL LTD
City/State/Country
Otniel Southern, IL
Establishment Address
149 Revava street,, Otniel Southern 9040700, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TWM- Tsadik Weiser Medical Ltd (Owner Number: 10092857)
Owner / Operator Contact Address
149 Revava street,, Otniel, IL-D 9040700, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K254060
PMA Number
N/A

All Registered Proprietary Names

LST - Life Saving Tourniquet LST - Life Saving Tourniquet

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2025-03-03
DXC Clamp, Vascular Cardiovascular Class 2 870.4450 2026-04-06

Official Correspondent

No official correspondent registered.

US Agent Details

Jack Ades Business: TW Medical Inc Email: Regulation@t-w-medical.com Phone: (917) 4538808

Related Public Records

Same Entity

TWM- Tsadik Weiser Medical Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038185753. Last updated year: 2026. Please use registration number 3038185753 when referencing this establishment in official correspondence.
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