Data / Medical devices / China / Ningbo Maxcon Medical Technology Co., Ltd
Ningbo Maxcon Medical Technology Co., Ltd: FDA-registered device maker in Ningbo Zhejiang, China, 4 510(k) clearances
Ningbo Maxcon Medical Technology Co., Ltd is registered with the FDA (registration 3013584693) in Ningbo Zhejiang, China. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated June 16, 2023. Registered through 2026. FDA data exported November 2, 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
- 3013584693
- Address
- No.30, Dongbei Rd, Dongqiao Town Yinzhou, Ningbo Zhejiang, China, 315157
- Owner or operator
- Ningbo Maxcon Medical Technology Co., Ltd (10053789)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- March 3, 2019
- Registered through
- 2026
- Brand names listed
- MA1112,MA1211,MA1212,MA1213,MA1232,MA1324,MA1001,MA1002,MA1003,MA1010,MA1020,MA1030,3823-3437, MA1122,MA1311,MA1321,MA1352,MA1111,MA1121,MA1113, MA1221, Maxcon Chemotherapy Container (Model: MC1321), Maxcon Reusable Sharps container (MA1421, MA1411), Sharps container (ME1123)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Sharps | MMK | 2 | Contract manufacturer, Exporter to the US, 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 16, 2023 | K222906 | Maxcon Reusable Sharps Container, 17 Gallon Sharps Container MA1421 | MMK | Substantially Equivalent | Ningbo Maxcon Medical Technology Co., Ltd. | accessdata.fda.gov |
| June 1, 2023 | K222905 | Maxcon Sharps Container (1 QT Sharps Container, MA1112), Maxcon Sharps Container (5.4 QT Sharps Container, MA1212), Maxcon Sharps Container (5.4 QT Sharps Container, MA1213), Maxcon Sharps Container (7 Liter Sharps Container, MA1324) | MMK | Substantially Equivalent | Ningbo Maxcon Medical Technology Co., Ltd. | accessdata.fda.gov |
| January 3, 2019 | K180984 | Maxcon Sharps Container | MMK | Substantially Equivalent | Ningbo Maxcon Medical Technology Co., Ltd. | accessdata.fda.gov |
| January 3, 2019 | K180983 | Maxcon Two Gallon Chemotherapy Container | MMK | Substantially Equivalent | Ningbo Maxcon Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 16, 2023. 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.