Swank Plus, Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 3
What Swank Plus, Ltd. makes
Swank Plus, Ltd. manufactures spectacle frames, magnifying spectacles, and nonprescription sunglasses.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Frame, Spectacle Ref K873965
Regimes: 510(k) Registry: 510(k)Spectacle, Magnifying Ref K873967
Regimes: 510(k) Registry: 510(k)Sunglasses (Nonprescription) Ref K873966
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Swank Plus, Ltd. have in the registry?
The registry currently lists 3 devices for Swank Plus, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Swank Plus, Ltd.'s devices?
Among its 3 most recently registered devices, Swank Plus, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Swank Plus, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Swank Plus, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Swank Plus, Ltd. in the registry?
The most recently registered devices listed for Swank Plus, Ltd. include FRAME, SPECTACLE, SPECTACLE, MAGNIFYING and SUNGLASSES (NONPRESCRIPTION).