Data / Medical devices / China / HONSUN (NANTONG) Co., Ltd.
HONSUN (NANTONG) Co., Ltd.: FDA-registered device maker in Nantong Jiangsu, China, 13 510(k) clearances
HONSUN (NANTONG) Co., Ltd. is registered with the FDA (registration 3007740533) in Nantong Jiangsu, China. It lists 9 device types. The FDA files 13 510(k) clearances under its listings, the newest dated June 17, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007740533
- Address
- NO.8, Tongxing Road, Nantong Economic & Technological Development Area, Nantong Jiangsu, China, 226009
- Owner or operator
- HONSUN (NANTONG) Co., Ltd. (10029908)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- July 14, 2009
- Registered through
- 2026
- Brand names listed
- AC Compressor Nebulizer (Model:NB-210C,NB-211C,NB-212C,NB-213C,NB-215C,NB-219C,NB-220C,NB-221C,NB-222C,NB-235C), Aneroid sphygmomanometer(HS-20A, HS-20D,HS-201W,HS-201Y,HS-201C1,HS-201Q3,HS-50B,HS-50C,HS-50D, Blood pressure Kit, Blood pressure Kit(model:7104,7105,7106,7107,7108,7109,7100,7099), Blood pressure Kit(model:BP-01), Blood pressure Kit(model:DS-9197-BK, DS-9181-BK), Blood pressure Kit(model:EBS-330, EBS-311, EBP-540), Blood pressure Kit(model:SPS-120, SP-110) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Compressor, Air, Portable | BTI | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Generator, Oxygen, Portable | CAW | 2 | Manufacturer | accessdata.fda.gov |
| Mask, Gas, Anesthetic | BSJ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Mouthpiece, Breathing | BYP | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Pump, Nebulizer, Electrically Powered | JPW | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Contract manufacturer, 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 17, 2026 | K252399 | Portable Oxygen Concentrator | CAW | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| April 28, 2026 | K260260 | Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569) | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| October 9, 2025 | K251795 | Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| April 6, 2020 | K192500 | Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer | DXQ | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| February 21, 2018 | K170866 | Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579 | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| October 27, 2017 | K170466 | Automatic Blood Pressure Monitor Model LD-518 & LD-537 | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| October 25, 2017 | K170454 | Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| January 8, 2015 | K140237 | DISPOSABLE NEBULIZER SET | CAF | Substantially Equivalent | Suzhou Weikang Medical Apparatus Co., Ltd. | accessdata.fda.gov |
| October 23, 2013 | K132627 | AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| September 12, 2013 | K130925 | AUTOMATIC BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| July 8, 2013 | K131463 | WRIST AUTOMATIC BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
| November 10, 2009 | K091272 | BESMED JET NEBULIZER BOTTLE SET | CAF | Substantially Equivalent | Besmed Health Business Corp | accessdata.fda.gov |
| October 28, 2009 | K092245 | ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100 | DXQ | Substantially Equivalent | Honsun (Nantong) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Pump, Nebulizer, Electrically Powered
- All makers of Mask, Gas, Anesthetic
- All makers of Blood Pressure Cuff
- All makers of Compressor, Air, Portable
Updated June 17, 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.