Data / Medical devices / China / Ningbo Albert Novosino Co., Ltd.
Ningbo Albert Novosino Co., Ltd.: FDA-registered device maker in Yuyao Zhejiang, China, 2 510(k) clearances
Ningbo Albert Novosino Co., Ltd. is registered with the FDA (registration 3011209790) in Yuyao Zhejiang, China. It lists 17 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 9, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011209790
- Address
- No.1206 Qingfeng West Road, Sanqishi Town, Yuyao Zhejiang, China, 315412
- Owner or operator
- Ningbo Albert Novosino Co., Ltd. (10025343)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- April 8, 2008
- Registered through
- 2026
- Brand names listed
- Breast Pump, Disposable Blood Pressure Cuff; Reusable Blood Pressure Cuff, Dropper, Ear Pain Relief Device, Ear Pressure Relief Device, Ear Syringe, Ear irrigation kit, Endoscope Insufflation Bulb and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Single Patient Use, Portable, Nonpowered | GCY | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Blood Pressure Cuff | DXQ | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bulb, Inflation, For Endoscope | FCY | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Device, Inflation, Middle Ear | MJV | U | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Douche Apparatus, Vaginal, Therapeutic | HED | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Dropper, Ent | KCM | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Ear Irrigation Kit | OGQ | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Enema Kit | FCE | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Infusor, Pressure, For I.V. Bags | KZD | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Irrigator, Powered Nasal | KMA | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Powered Inflatable Tube | IRP | 2 | Contract manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Otoscope | ERA | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Pump, Breast, Non-Powered | HGY | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Sleeve, Limb, Compressible | JOW | 2 | Contract manufacturer | accessdata.fda.gov |
| Syringe, Ent | KCP | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | 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 9, 2023 | K230502 | Ear Pressure Relief Device(Model:ER813B) | MJV | Substantially Equivalent | Ningbo Albert Novosino Co., Ltd. | accessdata.fda.gov |
| November 20, 2017 | K173044 | Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff | DXQ | Substantially Equivalent | Ningbo Albert Novosino Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Blood Pressure Cuff
- All makers of Pump, Breast, Non-Powered
- All makers of Ear Irrigation Kit
- All makers of Apparatus, Suction, Single Patient Use, Portable, Nonpowered
- All makers of Bulb, Inflation, For Endoscope
- All makers of Sleeve, Limb, Compressible
Updated June 9, 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.