Skip to the page

Data / Medical devices / China / Unimed Medical Supplies Inc

Unimed Medical Supplies Inc: FDA-registered device maker in Shenzhen Guangdong, China, 23 510(k) clearances

Unimed Medical Supplies Inc is registered with the FDA (registration 3007307487) in Shenzhen Guangdong, China. It lists 15 device types. The FDA files 23 510(k) clearances under its listings, the newest dated April 14, 2026. Registered through 2027. FDA data exported November 3, 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.

FDA registration number
3007307487
Address
Bld #8,Nangang 3rd Industrial park, tangtou, shiyan, Baoan, Shenzhen Guangdong, China, 518108
Owner or operator
Unimed Medical Supplies Inc (10027206)
Roles
Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
First device listed
October 13, 2008
Registered through
2027
Brand names listed
0-05-0065-U, 0-05-0066-U, 0-05-0071, 0-05-0072-U, 0-05-0073-U, 0-05-0074-U, 0-05-0075-U, 0-05-0076-U and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 14, 2026K260931Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
January 9, 2026K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)DXQSubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
December 1, 2025K251696Unimed Reusable SpO2 Sensors (-48 Series and -29 Series) (U410-48); Unimed Reusable SpO2 Sensors (-48 Series and -29 Series) (U410-29)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
December 1, 2025K251691Unimed Reusable SpO2 Sensors (-08 Series) (U403S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U203S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U103S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U103-08)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
November 18, 2025K251695Unimed Reusable SpO2 Sensors (-06 Series) (U403S-06); Unimed Reusable SpO2 Sensors (-06 Series) (U203S-06); Unimed Reusable SpO2 Sensors (-06 Series) (U103S-06)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
November 18, 2025K251693Unimed Reusable SpO2 Sensors (-75 Series) (U410-75); Unimed Reusable SpO2 Sensors (-75 Series) (U110-75); Unimed Reusable SpO2 Sensors (-75 Series) (U410S-75); Unimed Reusable SpO2 Sensors (-75 Series) (U110S-75); Unimed Reusable SpO2 Sensors (-75 Series) (U210S-75)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
August 13, 2025K250931Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U403-117); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U103-117); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U410-121); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U110-121)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
July 15, 2025K251045Disposable Neonatal NIBP Cuff (U1682S-C51N); Disposable Neonatal NIBP Cuff (U1683S-C51N); Disposable Neonatal NIBP Cuff (U1684S-C51N); Disposable Neonatal NIBP Cuff (U1685S-C51N)DXQSubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
February 20, 2025K243086Unimed Reusable Finger Clip SpO2 Sensors (UXXX-91 Series) (U403-91); Unimed Reusable Finger Clip SpO2 Sensors (UXXX-91 Series) (U410-91)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
February 6, 2025K242580Unimed Reusable Finger Clip SpO2 Sensors (U103-125); Unimed Reusable Finger Clip SpO2 Sensors (U403-254); Unimed Reusable Finger Clip SpO2 Sensors (U103-254); Unimed Reusable Finger Clip SpO2 Sensors (U403-125)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
December 19, 2022K222213Pulse Oximeter (UC-200, UC-201, UC-202, UC-203, UC-204, UC-100, UC-101, UC-102, UC-103, UC-104)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
March 4, 2021K210019Unimed CO2 Mainstream Module Model Capno-M, Unimed CO2 Mainstream Module Model Capno-M+CCKSubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
October 31, 2016K152472Disposable Pressure TransducerDRSSubstantially EquivalentZhejiang Haisheng Medical Device Co., Ltd.accessdata.fda.gov
February 6, 2015K142832Unimed Disposable and Reusable SPO2 SensorsDQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
November 4, 2014K142489Unimed Disposable ECG lead wiresDSASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
May 29, 2012K121427UNIMED TEMPERATURE PROBEFLLSubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
May 4, 2012K120364UNIMED DISPOSABLE BLOOD PRESSURE CUFFDXQSubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
November 22, 2011K112544UNIMED BLOOD PRESSURE CUFFDXQSubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
August 20, 2009K083448CABLE, TRANSDUCER, MODEL 2400GNDQASubstantially EquivalentConmed Corporationaccessdata.fda.gov
December 2, 2008K082546REUSABLE OHMEDA (U410-02), DATEX (U410-09) COMPATABLE ADULT FINGER CLIP SENSOR, PHILLIPS ADULT SOFT TIP SENSOR(U403S-91)DQASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
October 10, 2008K082959PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORSDSASubstantially EquivalentUnimed Medical Supplies, Inc.accessdata.fda.gov
September 15, 2004K041954DISPOSABLE MONITORING ELECTRODESDRXSubstantially EquivalentShanghai Intco Electrode Manufacturing Co., Ltd.accessdata.fda.gov
December 15, 2000K002384M-XX OXYGEN SENSORSCCLSubstantially EquivalentInternational Business Strategiesaccessdata.fda.gov

Compare with other makers

Updated April 14, 2026. 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.