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Data / Medical devices / Regulator, Temperature

Regulator, Temperature (JRR): 9 FDA-registered makers in 5 countries

9 establishments in 5 countries are registered with the FDA to make Regulator, Temperature (product code JRR, Class 1, 21 CFR 862.2050). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on August 5, 1982, and lists 0 recall events (0 Class I). FDA data exported November 3, 2026.

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Product code
JRR
Device class
1
Regulation
862.2050
Medical specialty
Clinical Chemistry

Makers by country

CountryMakers
China3
United States3
India1
France1
Singapore1

Makers of Regulator, Temperature

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Accuster Technologies Pvt. Ltd.New Delhi, IndiaManufacturer0000api.fda.gov
Bio-RadMARNES-LA-COQUETTE Ile-de-France, FranceSpecification developer0000api.fda.gov
Bio-Rad Laboratories (Singapore) Pte. Ltd.Singapore Central Singapore, SingaporeContract manufacturer0000api.fda.gov
Infitek Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Labpeak Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
LCR Hallcrest, LLC. (IL)Glenview, IL, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Nico CorporationIndianapolis, IN, United StatesSpecification developer0000api.fda.gov
Primo Medical Group, IncW Bridgewater, MA, United StatesContract manufacturer0000api.fda.gov
Scitek Global Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov

Updated August 5, 1982. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.