TEMPDROP LTD.

FDA Device Registration & Listing · Tel Aviv, IL · Registration 3016099071

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
3016099071
FEI Number
3016099071
Entity Name
TEMPDROP LTD.
City/State/Country
Tel Aviv, IL
Establishment Address
Ha'shlosha 2, Entrance D, Brain Embassy, Tel Aviv 6706054, IL
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Tempdrop Ltd. (Owner Number: 10061735)
Owner / Operator Contact Address
Ha'shlosha 2, Entrance D, Brain Embassy, Tel Aviv, IL-TA 6706054, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LHD Device, Fertility Diagnostic, Proceptive Unknown Class U N/A 2019-11-19

Official Correspondent

Liz Schindel

US Agent Details

Elor Kahalani Email: eli@logystico.com Phone: (732) 3028989

Related Public Records

Same Entity

Tempdrop 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 3016099071. Last updated year: 2026. Please use registration number 3016099071 when referencing this establishment in official correspondence.
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