Data / Medical devices / China / Shenzhen Jumper Medical Equipment Co.,Ltd.
Shenzhen Jumper Medical Equipment Co.,Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 13 510(k) clearances
Shenzhen Jumper Medical Equipment Co.,Ltd. is registered with the FDA (registration 3008973759) in Shenzhen Guangdong, China. It lists 9 device types. The FDA files 13 510(k) clearances under its listings, the newest dated October 27, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3008973759
- Address
- D Building, No. 71, Xintian Road, Fuyong Street Baoan, Shenzhen Guangdong, China, 518103
- Owner or operator
- Shenzhen Jumper Medical Equipment Co., Ltd. (10035564)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- March 6, 2011
- Registered through
- 2026
- Brand names listed
- ADF-B06 Andesfit, AE174, AMS PROOF Electronic Blood Pressure Monitor ( AMS 101 US), Body Fat Scale, JPD-BFS100, JPD-BFS101, JPD-BFS102, JPD-BFS200A, JPD-BFS200B, JPD-BFS200D, JPD-BFS710, JPD-BFS711, Body Fat Scale,JPD-700C, Easy@Home Blood Pressure Monitor (EBP-020), Electronic Blood Pressure Monitor JPD-900A, Electronic Blood Pressure Monitor JPD-900W and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition, Exempt | PUH | 2 | Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Monitor, Ultrasonic, Fetal | KNG | 2 | Manufacturer | accessdata.fda.gov |
| Oximeter | DQA | 2 | Manufacturer | accessdata.fda.gov |
| Oximeter, Infrared, Sporting, Aviation | OCH | 2 | Manufacturer | accessdata.fda.gov |
| Oximeter, Wellness | PGJ | 2 | Manufacturer | accessdata.fda.gov |
| Scale, Stand-On, Patient | FRI | 1 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 27, 2023 | K231310 | Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| August 1, 2019 | K182871 | Mini TENS Therapy Device | NUH | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| May 5, 2019 | K182437 | Wireless Intelligent Thermometer | FLL | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| March 3, 2019 | K182495 | Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| March 14, 2018 | K172795 | Infrared Thermometer | FLL | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| November 3, 2017 | K170965 | Fingertip Pulse Oximeter | DQA | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| October 13, 2017 | K170151 | Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Pango Electronic Co., Ltd. | accessdata.fda.gov |
| July 31, 2017 | K161845 | Electronic Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Pango Electronic Co., Ltd. | accessdata.fda.gov |
| August 28, 2014 | K140582 | FINGERTIP PULSE OXIMETER | DQA | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| January 24, 2014 | K131457 | FETAL ULTRASONIC MONITOR AND ACCESSORIES | KNG | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| November 12, 2013 | K131243 | NON-CONTACT INFRARED THERMOMETER | FLL | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
| June 14, 2013 | K131569 | PG-800A SERIES | DXN | Substantially Equivalent | Shenzhen Pango Electronic Co., Ltd. | accessdata.fda.gov |
| February 4, 2011 | K110124 | FETAL DOPPLER JPD-100S | KNG | Substantially Equivalent | Shenzhen Jumper Medical Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Analyzer, Body Composition, Exempt
- All makers of Continuous Measurement Thermometer
- All makers of Oximeter, Wellness
- All makers of Scale, Stand-On, Patient
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Oximeter
Updated October 27, 2023. 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.