Data / Medical devices / Hong Kong / P L Overseas Limited
P L Overseas Limited: FDA-registered device maker in Hong Kong, Hong Kong, 1 510(k) clearance
P L Overseas Limited is registered with the FDA (registration 3014254835) in Hong Kong, Hong Kong. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 30, 2017. 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
- 3014254835
- Address
- Flat / RM 1101 BLK 1 11F, Cheung Sha Wan Plaza, 833 Cheung Sha Wan Road, Laz Chi Kok, Hong Kong, Hong Kong, 999077
- Owner or operator
- P L Overseas Limited (10056522)
- Roles
- Exporter to the US, Foreign private label distributor, Manufacturer, Specification developer
- First device listed
- December 19, 2017
- Registered through
- 2026
- Brand names listed
- Contact Lens Case, Dispenser, solid medication
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Case, Contact Lens | LRX | 2 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Foreign private label distributor, 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 |
|---|---|---|---|---|---|---|
| November 30, 2017 | K172925 | Contact Lens Case, Model: A-1, B-1 | LRX | Substantially Equivalent | P L Overseas Limited | accessdata.fda.gov |
Compare with other makers
Updated November 30, 2017. 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.