Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012381649

FEI Number

3012381649

Entity Name

TEMPRAMED

City/State/Country

Sammamish, WA, US

Establishment Address

19481 SE 14th St, Sammamish, WA 98075, US

Establishment Type(s)

Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

TempraMed Inc (Owner Number: 10052028)

Owner / Operator Contact Address

64 HEH BIYAR, TEL AVIV-YAFO, IL-TA 6219812, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ViVi cap1 VIVI EPI VIVI Med VIVI Cap

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQG	Adaptor, Holder, Syringe	Physical Medicine	Class 1	890.5050	2016-06-02

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TempraMed Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3014384423	TempraMed Israel Ltd.	Tel Aviv, IL

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012381649. Last updated year: 2026. Please use registration number 3012381649 when referencing this establishment in official correspondence.