Data / Medical devices / China / Nanning Baolai Medical Instrument Co., Ltd
Nanning Baolai Medical Instrument Co., Ltd: FDA-registered device maker in NANNING Guangxi, China, 1 510(k) clearance
Nanning Baolai Medical Instrument Co., Ltd is registered with the FDA (registration 3008615394) in NANNING Guangxi, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 6, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008615394
- Address
- 5th Floor, No.8 Building, Phase II, China-ASEAN Technology Enterprise Incubation Base No.3 Zongbu Road, Xixiangtang District, NANNING Guangxi, China, 530007
- Owner or operator
- NANNING BAOLAI MEDICAL INSTRUMENT CO., LTD (10049130)
- Roles
- Manufacturer
- First device listed
- April 17, 2015
- Registered through
- 2026
- Brand names listed
- BD2, CD1; CD2 ;CD3, Extraoral suction system model: ESS1, Face Shield (Model: FS-A), Face Shield (Model: FS-B), GL5,GL5L, K10, Non-surgical Mask and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Scaler, Ultrasonic | ELC | 2 | Manufacturer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Suction Operatory | EBR | 1 | 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 6, 2015 | K140233 | ULTRASONIC SCALER | ELC | Substantially Equivalent | Nanning Baolai Medical Instrument Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Scaler, Ultrasonic
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- All makers of Accessory, Surgical Apparel
- All makers of Unit, Suction Operatory
Updated April 6, 2015. 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.