Ptech Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Ptech Co., Ltd. makes
Ptech Co., Ltd. manufactures intradermal and transdermal pain management devices, including PainTB for subcutaneous administration and PainTJ for transdermal delivery.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
PainTB, PainTJ Ref K203337
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ptech Co., Ltd. have in the registry?
The registry currently lists 1 device for Ptech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ptech Co., Ltd.'s devices?
Among its 1 most recently registered device, Ptech Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ptech Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ptech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ptech Co., Ltd. in the registry?
The most recently registered devices listed for Ptech Co., Ltd. include PainTB, PainTJ.