Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017170064

FEI Number

3017170064

Entity Name

UAB Life Instruments

City/State/Country

Skaidiskes Vilniaus Apskritis, LT

Establishment Address

Sodu 8, Skaidiskes Vilniaus Apskritis 13269, LT

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

UAB "Life Instruments" (Owner Number: 10075969)

Owner / Operator Contact Address

Sodu 8, Skaidiskes, LT-VL 13269, LT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

K-System Origio

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PUB	Accessory, Assisted Reproduction, Exempt	Obstetrics/Gynecology	Class 2	884.6120	2020-07-02

Official Correspondent

Monika Naudziuviene

US Agent Details

BRIAN SZEREMETA Business: COOPERSURGICAL Email: FURLS-Codes@coopersurgical.com Phone: (203) 6015200

Related Public Records

Same Entity

UAB "Life Instruments"

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

View Entity Profile →

Similar Registrations

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3009747883	Esco Medical Technologies, UAB	Ramuciai Kauno Apskritis, LT
3007459332	ASTEC CO., Ltd.	Kasuya Fukuoka, JP
3003244268	CRYO BIO SYSTEM	Saint Ouen sur Iton Orne, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017170064. Last updated year: 2026. Please use registration number 3017170064 when referencing this establishment in official correspondence.