Data / Medical devices / China / Dolanvy (Suzhou) Medical Technology Co., Ltd
Dolanvy (Suzhou) Medical Technology Co., Ltd: FDA-registered device maker in Suzhou Jiangsu, China, 1 510(k) clearance
Dolanvy (Suzhou) Medical Technology Co., Ltd is registered with the FDA (registration 3025376109) in Suzhou Jiangsu, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 28, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3025376109
- Address
- Room 102, Building 8, No. 258, Shengpu Road, Suzhou Industrial Park, Suzhou Jiangsu, China, 215000
- Owner or operator
- Dolanvy (Suzhou) Medical Technology Co., Ltd (10086351)
- Roles
- Manufacturer
- First device listed
- November 2, 2022
- Registered through
- 2026
- Brand names listed
- Maptag MP-3521 Household Male Sexual Function Rehabilitation Therapy Apparatus,, Maptag MP-3522 Household Male Sexual Function Rehabilitation Therapy Apparatus,, Maptag Male Sexual Function Rehabilitation Therapy Apparatus, Include 3 Models,, Maptag Muscle Massage Gun, Maptag Neck Massager, Pocket Massager, Maptag SW-3503 Male Sexual Function Rehabilitation Therapy Apparatus, Nocturnal Penile Tumescence Apparatus: SW-3620, Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, External Penile Rigidity | LKY | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Stimulator, Electrical, Non-Implantable, For Incontinence | KPI | 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 |
|---|---|---|---|---|---|---|
| April 28, 2026 | K252831 | Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927) | KPI | Substantially Equivalent | Dolanvy (Suzhou) Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Electrical, Non-Implantable, For Incontinence
- All makers of Device, External Penile Rigidity
- All makers of Massager, Therapeutic, Electric
Updated April 28, 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.