Data / Medical devices / Vietnam / Mullan Medical (vietnam) Limited Company
Mullan Medical (vietnam) Limited Company: FDA-registered device maker in Tu Son Bac Ninh, Vietnam, 3 510(k) clearances
Mullan Medical (vietnam) Limited Company is registered with the FDA (registration 3029973920) in Tu Son Bac Ninh, Vietnam. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 19, 2016. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3029973920
- Address
- 5th floor, High-rise Factory - Block 1, No. 2, BH5 Street, VSIP Bac Ninh, Phu Chan Ward, Tu Son Bac Ninh Province, Vietnam, Tu Son Bac Ninh, Vietnam, 16000
- Owner or operator
- Top-Rank Health Care Co. Ltd (10089230)
- Roles
- Manufacturer
- First device listed
- November 17, 2023
- Registered through
- 2026
- Brand names listed
- Adhesive Electrodes, Electrosurgical Disposable Grounding Pads, MULLAN
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Manufacturer | accessdata.fda.gov |
| Electrosurgical Patient Return Electrode | ODR | 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 |
|---|---|---|---|---|---|---|
| August 19, 2016 | K160366 | Electrosurgical disposable grounding pads | ODR | Substantially Equivalent | Top-Rank Health Care Co., Ltd. | accessdata.fda.gov |
| November 22, 2013 | K132588 | ADHESIVE ELECTRODES | GXY | Substantially Equivalent | Top-Rank Health Care Equipment Co., Ltd. | accessdata.fda.gov |
| May 7, 2007 | K070612 | TOP-RANK ADHESIVE ELECTRODE | GXY | Substantially Equivalent | Top-Rank Health Care Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 19, 2016. 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.