Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1424489

FEI Number

3002729000

Entity Name

LCR Hallcrest, LLC. (IL)

City/State/Country

GLENVIEW, IL, US

Establishment Address

1911 Pickwick Ln, GLENVIEW, IL 60026, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LCR Hallcrest, LLC. (Owner Number: 9037996)

Owner / Operator Contact Address

1911 PICKWICK LANE, --, Glenview, IL 60026, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

BK830006

PMA Number

N/A

All Registered Proprietary Names

CRYSTALINE Brand Temperature Trend Indicator, Model No. 5105 DERMATHERM Brand Perfusion Band, Model 2100 PB Series TempStrip(tm) Brand Temperature Trend Indicator, Model No. 8104 SHARN CRYSTALINE II DERMATHERM Brand Perfusion Strip, Model 2200 PS SHARN TEMPALERT II TempAlertTMJI Brand Temperature Trend Indicator SHARN CRYSTALINE W CRYSTALINE ST Brand Temperature Trend Indicator, Model No. 6102 Accubar CLINITREND THERMOSTRIP TempTrend II FEVERTEMP EZ-Temp II (TM) ANESTHESIA MONITOR FEVERSCAN CLINITEMP DIGITEMP TempTrend BRITEVENT BRITELINE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KSE	Refrigerator, Freezer, Blood Storage	Hematology	Class 2	864.9700	2021-09-27
KPD	Strip, Temperature, Forehead, Liquid Crystal	General Hospital	Class 2	880.2200	2002-03-20
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	Clinical Chemistry	Class 1	862.2050	2006-10-24
JRR	Regulator, Temperature	Clinical Chemistry	Class 1	862.2050	2021-12-30
KSS	Supplies, Blood-Bank	Hematology	Class 1	864.9050	2021-08-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LCR Hallcrest, LLC.

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2008	Beckman Coulter Inc	1	FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013	Biomerieux Inc	1	PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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3027645317	INFITEK CO., LTD.	Shanghai, CN
3017882410	BIOTECNO INDUSTRIA E COMERCIO LTDA	SANTA ROSA Rio Grande do Sul, BR
3004973569	HELMER Inc.	NOBLESVILLE, IN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1424489. Last updated year: 2026. Please use registration number 1424489 when referencing this establishment in official correspondence.