Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027691164

FEI Number

3027691164

Entity Name

LTS DEVICE TECHNOLOGIES

City/State/Country

Netanya Central, IL

Establishment Address

29 Yad Harutzim St., Netanya Central 4250529, IL

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

LTS Device Technologies (Owner Number: 10088332)

Owner / Operator Contact Address

29 Yad Harutzim St., Netanya, IL-M 4250529, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Colombia OBI Commercial Sterilized

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QLF	On-Body Injector	General Hospital	Class 2	880.5860	2023-08-01

Official Correspondent

No official correspondent registered.

US Agent Details

Steve Leno Email: Steve.Leno@ltslohmann.com Phone: (651) 5525622

Related Public Records

Same Entity

LTS Device Technologies

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3016603289	Apellis	Waltham, MA, US
2032861	West Pharmaceutical Services Arizona, Inc.	Tempe, AZ, US
2032862	West Pharmaceutical Services AZ, Inc.	SCOTTSDALE, AZ, US
3012484616	ENABLE INJECTIONS	Cincinnati, OH, US
3008816891	A+ SECURE PACKAGING	La Vergne, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027691164. Last updated year: 2026. Please use registration number 3027691164 when referencing this establishment in official correspondence.