Data / Medical devices / China / Ningbo Kaida Rubber And Plastic Technology Co., Ltd
Ningbo Kaida Rubber And Plastic Technology Co., Ltd: FDA-registered device maker in Yu Yao City, Zhejiang Province, China, 1 510(k) clearance
Ningbo Kaida Rubber And Plastic Technology Co., Ltd is registered with the FDA (registration 3006633372) in Yu Yao City, Zhejiang Province, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 1, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006633372
- Address
- No. 1 Qinggang Industrial Park Mou Shan Town, Yu Yao City, Zhejiang Province, China, 315456
- Owner or operator
- NINGBO KAIDA RUBBER AND PLASTIC TECHNOLOGY CO., LTD (9100523)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- May 21, 2007
- Registered through
- 2026
- Brand names listed
- CASE, CONTACT LENS, Contact Lens Accessories, Contact Lens Applicator (Inserter/Remover), Silicone Contact Lens Applicator (Inserter/Remover)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Case, Contact Lens | LRX | 2 | Manufacturer | accessdata.fda.gov |
| Inserter/Remover Contact Lens | KYE | 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 |
|---|---|---|---|---|---|---|
| May 1, 2007 | K071081 | CONTACT LENS CASE | LRX | Substantially Equivalent | Ningbo Kaida Rubber and Plastic Technology Co., LT | accessdata.fda.gov |
Compare with other makers
Updated May 1, 2007. 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.