Data / Medical devices / China / Dongguan Mars Medical Products Co., Ltd.
Dongguan Mars Medical Products Co., Ltd.: FDA-registered device maker in Dongguan City Guangdong, China, 4 510(k) clearances
Dongguan Mars Medical Products Co., Ltd. is registered with the FDA (registration 9615583) in Dongguan City Guangdong, China. It lists 9 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 18, 2019. Registered through 2026. 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
- 9615583
- FEI number
- 3003171455
- Address
- Room 301, 2nd Building, 6# Manfeng Industrial West Road One Shatian Town, Dongguan City Guangdong, China, 523993
- Owner or operator
- Dongguan Mars Medical Products Co., Ltd (10028732)
- Roles
- Manufacturer
- First device listed
- March 1, 2009
- Registered through
- 2026
- Brand names listed
- Clinical electronic thermometer,MARS-E-01, IBD, MARS, Mars, Medical disposable face mask, N95 MASK, Omni Original
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Elastic | FQM | 1 | Manufacturer | accessdata.fda.gov |
| Blood Pressure Cuff | DXQ | 2 | Manufacturer | accessdata.fda.gov |
| Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua | QKR | N | Manufacturer | accessdata.fda.gov |
| Flowmeter, Blood, Cardiovascular | DPW | 2 | Manufacturer | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Manufacturer | accessdata.fda.gov |
| Respirator, Surgical | MSH | 2 | Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Manufacturer | accessdata.fda.gov |
| Thermometer Kit | PXH | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| June 18, 2019 | K191209 | Aneroid Type Blood Pressure Kit | DXQ | Substantially Equivalent | Dongguan Mars Medical Products Co., Ltd. | accessdata.fda.gov |
| December 10, 2004 | K032825 | VITAL VISION ARTERIAL HARDNESS AND BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Mars Medical Products Co., Ltd. | accessdata.fda.gov |
| December 14, 1998 | K980845 | MS-900S, MS-900SPM & MS-900SFM | DXN | Substantially Equivalent | Mars Medical Products | accessdata.fda.gov |
| March 13, 1998 | K972213 | MS-700 | DPW | Substantially Equivalent | Alan S. Lee | accessdata.fda.gov |
Compare with other makers
- All makers of Respirator, Surgical
- All makers of Mask, Scavenging
- All makers of Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
- All makers of Flowmeter, Blood, Cardiovascular
- All makers of Tape And Bandage, Adhesive
- All makers of Blood Pressure Cuff
Updated June 18, 2019. 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.