Jieying Laboratory, Inc.
Country not established
- Devices
- 1
What Jieying Laboratory, Inc. makes
Jieying Laboratory, Inc. manufactures pipettes for medical and laboratory use, including injection, holding, biopsy, denuding, and partial zona dissection (PZD) pipettes, as well as assisted hatching (HA) pipettes. These devices are designed for precise fluid handling and reproductive procedures in clinical settings.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway. The portfolio is regulated under US medical device laws, with no additional international registries specified. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jieying Laboratory, Inc. have in the registry?
The registry currently lists 1 device for Jieying Laboratory, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jieying Laboratory, Inc.'s devices?
Among its 1 most recently registered device, Jieying Laboratory, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jieying Laboratory, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jieying Laboratory, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jieying Laboratory, Inc. in the registry?
The most recently registered devices listed for Jieying Laboratory, Inc. include INJECTION PIPETTE; HOLDING PIPETTE; BIOPSY PIPETTE; DENUDING PIPETTE; PARTIAL ZONA DISSECTION (PZD) PIPETTE; ASSISTED HA.