Data / Medical devices / System, Pressure Measurement, Intermittent

System, Pressure Measurement, Intermittent (JFC): 35 FDA-registered makers in 15 countries

Name: FDA-registered makers of System, Pressure Measurement, Intermittent
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

35 establishments in 15 countries are registered with the FDA to make System, Pressure Measurement, Intermittent (product code JFC, Class 1, 21 CFR 890.1600). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 11 510(k) clearances under this code, the latest on May 12, 1993, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get every maker of this device Makers in the United States Watch this device

Product code: JFC
Device class: 1
Regulation: 890.1600
Medical specialty: Physical Medicine

Makers by country

Country	Makers
United States	11
China	7
Mexico	2
Ireland	2
Germany	2
Switzerland	2
Spain	1
Slovenia	1
Australia	1
Belgium	1
India	1
Argentina	1
South Korea	1
Israel	1
Canada	1

Makers of System, Pressure Measurement, Intermittent

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.

Maker	Location	Role	Source
Blue Chip Medical Products, Inc.	Suffern, NY, United States	Manufacturer	api.fda.gov
C&S Manufacturing International SRL de CV	Torreon Coahuila, Mexico	Manufacturer	api.fda.gov
Clinical Image Retrieval Systems, Inc.	Franklin, NJ, United States	Manufacturer	api.fda.gov
Danu Medical	Dublin Dublin(County), Ireland	Manufacturer	api.fda.gov
Diers International GMBH	Mainz-Kastel Hesse, Germany	Manufacturer	api.fda.gov
DJ Orthopedics De Mexico, S.A. De C.V.	TIJUANA Baja California, Mexico	Manufacturer	api.fda.gov
Djo, LLC	Carlsbad, CA, United States	Specification developer	api.fda.gov
Feeltect Ltd	Spiddal Galway(County), Ireland	Manufacturer	api.fda.gov
Fourier Intelligence Inc.	Shanghai, China	Manufacturer	api.fda.gov
Instituto De Investigacion En Ortopedia Avanzada S.L	Cuarte Huesca, Spain	Manufacturer	api.fda.gov
L-Tek D.O.O.	Sentjernej Ljubljana, Slovenia	Contract manufacturer	api.fda.gov
Lenexa Medical Pty Ltd	Balwyn Victoria, Australia	Manufacturer, Specification developer	api.fda.gov
Linus Health, Inc.	Boston, MA, United States	Manufacturer	api.fda.gov
Macmed Technology Inc.	Shenzhen Guangdong, China	Manufacturer	api.fda.gov
Magnes AG	Zurich, Switzerland	Specification developer	api.fda.gov
Med-Linket Corp	Alhambra, CA, United States	Manufacturer	api.fda.gov
Materialise Motion N.V.	Paal Limburg, Belgium	Manufacturer	api.fda.gov
Orantech Inc.	Shenzhen Guangdong, China	Manufacturer	api.fda.gov
P Bhogilal Pvt Ltd	Kolkata West Bengal, India	Manufacturer	api.fda.gov
Pampamed SRL	Buenos Aires, Argentina	Complaint file establishment, Manufacturer	api.fda.gov
Pearl Technology AG	Schlieren Zurich, Switzerland	Complaint file establishment, Manufacturer	api.fda.gov
ROHO, Inc.	Belleville, IL, United States	Complaint file establishment, Manufacturer	api.fda.gov
Salted Co., Ltd.	Hanam-si Gyeonggi, South Korea	Manufacturer	api.fda.gov
Shenzhen Med-Link Electronics Tech Co.,ltd	Shenzhen Guangdong, China	Manufacturer	api.fda.gov
Sportgait, Inc.	Wilmington, NC, United States	Manufacturer	api.fda.gov
T&T Medilogic Medizintechnik GMBH	Schoenefeld Brandenburg, Germany	Manufacturer	api.fda.gov
Tekscan, Inc.	Norwood, MA, United States	Manufacturer	api.fda.gov
Unimed Medical Supplies Inc	Shenzhen Guangdong, China	Manufacturer	api.fda.gov
Vibetech Enterprises, LLC	Sheboygan, WI, United States	Manufacturer	api.fda.gov
Wellsense Technologies Ltd.	Neve Ilan Jerusalem, Israel	Specification developer	api.fda.gov
Wellsense, Inc.	Rochester Hills, MI, United States	Manufacturer	api.fda.gov
Wenzhou Caretek Medical Device Co., Ltd	Wenzhou Zhejiang, China	Manufacturer	api.fda.gov
Wuhan ZJZK Technology Co.,ltd. (aka Wuhan ZJKC Technology Co.,ltd.)	Wuhan Hubei, China	Manufacturer	api.fda.gov
Xsensor Technology Corp.	CALGARY Alberta, Canada	Exporter to the US, Manufacturer	api.fda.gov
ZenoMetrics LLC	Peekskill, NY, United States	Manufacturer	api.fda.gov

Updated May 12, 1993. 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.