GERO3D LTD

FDA Device Registration & Listing · Tel Aviv-Yafo Central, IL · Registration 3029961128

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
3029961128
FEI Number
3029961128
Entity Name
GERO3D LTD
City/State/Country
Tel Aviv-Yafo Central, IL
Establishment Address
14, Weizman, Tel Aviv-Yafo Central 6423914, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Gero3D Ltd (Owner Number: 10089112)
Owner / Operator Contact Address
14 Weizmann st., Tel Aviv, IL-M 6423914, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

One splint S,M,L

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2023-11-07

Official Correspondent

Nadav Ichay

US Agent Details

Benzy Arazy Business: Medes USA C/O Matan Arazy Email: Medes@Arazygroup.com Phone: (415) 9921126

Related Public Records

Same Entity

Gero3D Ltd
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 3029961128. Last updated year: 2026. Please use registration number 3029961128 when referencing this establishment in official correspondence.
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