Jeil Tech Co., Ltd.
South KoreaFDA 510(k) applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Jeil Tech Co., Ltd. makes
Jeil Tech Co., Ltd. manufactures sterile, single-use low dead-volume (LDV) syringes designed for precise medication delivery in clinical and procedural settings. These syringes are engineered to minimize residual volume, ensuring accurate dosing of pharmaceuticals and reducing waste.
The company’s LDV syringes fall under FDA Class II regulatory classification and are listed via the 510(k) pathway in the United States. The devices are intended for use in medical environments where precise fluid administration is critical.
Catalogue
- 510(k) 510(k)
FDA establishments
- Jeil Tech Co., Ltd Sejong-si Daegu · KR FEI 3007774504
Frequently asked questions
How many devices does Jeil Tech Co., Ltd. have in the registry?
The registry currently lists 1 device for Jeil Tech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jeil Tech Co., Ltd.'s devices?
Among its 1 most recently registered device, Jeil Tech Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Jeil Tech Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jeil Tech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jeil Tech Co., Ltd. in the registry?
The most recently registered devices listed for Jeil Tech Co., Ltd. include Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe.
Which FDA establishments are linked to Jeil Tech Co., Ltd.?
1 FDA establishment is linked to Jeil Tech Co., Ltd. in the registry; they are listed on the company page.