LIFESIGN L.L.C.

FDA Device Registration & Listing · Skillman, NJ, US · Registration 2249224

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
2249224
FEI Number
3001835184
Entity Name
LIFESIGN L.L.C.
City/State/Country
Skillman, NJ, US
Establishment Address
85 Orchard Rd, Skillman, NJ 08558, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LIFESIGN L.L.C. (Owner Number: 9033809)
Owner / Operator Contact Address
85 ORCHARD ROAD, --, Skillman, NJ 08558, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Uricult CLED + MacConkey Uricult CLED/EMB

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JSH Culture Media, Non-Selective And Differential Microbiology Class 1 866.2320 2025-02-05

Official Correspondent

ROGER KANG

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIFESIGN L.L.C.
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 2249224. Last updated year: 2026. Please use registration number 2249224 when referencing this establishment in official correspondence.
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