Data / Medical devices / United States / Joicom Corporation
Joicom Corporation: FDA-registered device maker in Eastvale, CA, United States, 16 510(k) clearances
Joicom Corporation is registered with the FDA (registration 3015619973) in Eastvale, CA, United States. It lists 19 device types. The FDA files 16 510(k) clearances under its listings, the newest dated February 19, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3015619973
- Address
- 14129 The Merge Street, Building 3 Ste A, Eastvale, Eastvale, CA, United States, 92880
- Owner or operator
- Joicom Corporation (10060997)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- July 31, 2019
- Registered through
- 2026
- Brand names listed
- 2 in 1 Foot and Calf Massager:R-D002RS, Abdominal Massager:I-B-101, Air Compression Leg Massager : MM0521, MM0522,R-A2L, Blood Pressure Monitor: TMB-2276-B, Body Composition Scale:R-MSC04,R-MSB05,R-MSB04,F-MSC03,F-MSC02, R-MSC05,R-MSC06,R-MSC07,R-MSC08, Cordless Massager:EM-2016C, RP-EM2020C, Electric Cupping Massager: R-WMV01, Eye Massager: R-G002S, R-G003, R-G007, R-G011 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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 19, 2025 | K241578 | Wrist Digital Blood Pressure Monitor (BSX312, BSX313, BSX315, BSX322, BSX323, BSX353, BSX355) | DXN | Substantially Equivalent | Shenzhen Bsx Technology Electronics Co., Ltd. | accessdata.fda.gov |
| February 5, 2025 | K243555 | LED light therapy mask (E43, E32, E49B, E49C, E100B, E100C, E103B, E104B, E106A, E108A) | OLP | Substantially Equivalent | Shenzhen Eyco Technology Co., Ltd. | accessdata.fda.gov |
| November 20, 2024 | K232965 | Leg Massager (Models:RP-ALM070H, RP-ALM071H) | IRP | Substantially Equivalent | Shenzhen Ruiyi Business Technology Co., Ltd. | accessdata.fda.gov |
| September 17, 2024 | K240373 | Air compression Leg Massager (MM0520, MM0521, MM0522) | IRP | Substantially Equivalent | Zhangzhou Easepal Medical Science and Technology Co., Ltd. | accessdata.fda.gov |
| August 2, 2024 | K240981 | Air compression leg massager | IRP | Substantially Equivalent | Huizhou Xinyi Technology Co., Ltd. | accessdata.fda.gov |
| July 19, 2024 | K233067 | Wireless TENS & EMS (Model SM9110,SM9113,SM9116) | NUH | Substantially Equivalent | Chongqing Rob Linka Science and Technology Co., Ltd. | accessdata.fda.gov |
| April 29, 2024 | K240102 | Blood Pressure Monitor (TMB-2287-B) | DXN | Substantially Equivalent | Guangdong Transtek Medical Electronics Co., Ltd. | accessdata.fda.gov |
| February 12, 2024 | K233092 | Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W) | NUH | Substantially Equivalent | Chongqing Rob Linka Science and Technology Co., Ltd. | accessdata.fda.gov |
| November 28, 2023 | K232713 | Blood Pressure Monitor | DXN | Substantially Equivalent | Guangdong Transtek Medical Electronics Co., Ltd. | accessdata.fda.gov |
| March 28, 2023 | K223928 | Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K | OHT | Substantially Equivalent | Shenzhen Fansizhe Science and Technology Co., Ltd. | accessdata.fda.gov |
| March 15, 2023 | K222991 | Air Compression Leg Massager (model: EMK-701) | IRP | Substantially Equivalent | Xiamen Emoka Health Science & Technology Co., Ltd. | accessdata.fda.gov |
| December 23, 2022 | K222924 | Leg Massager RF-ALM070 | IRP | Substantially Equivalent | Shenzhen Ruiyi Business Technology Co., Ltd. | accessdata.fda.gov |
| December 8, 2022 | K221862 | YY-A02-B Overlapped Compression Therapy | IRP | Substantially Equivalent | Huizhou Xinyi Technology Co., Ltd. | accessdata.fda.gov |
| March 31, 2022 | K213745 | Air Compression Therapy Device, model: ST-502 | IRP | Substantially Equivalent | Shenzhen Future Electronic Co., Ltd. | accessdata.fda.gov |
| June 19, 2013 | K131395 | TRANSTEK BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Guangdong Transtek Medical Electronics Co., Ltd. | accessdata.fda.gov |
| January 31, 2012 | K120058 | TRANSTEK BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Zhongshan Transtek Electronics Co., Ltd. | accessdata.fda.gov |
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Updated February 19, 2025. 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.