Lilium Otsuka Co., Ltd.
JapanFDA applicant, unverified
- Devices
- 1
What Lilium Otsuka Co., Ltd. makes
Lilium Otsuka Co., Ltd. manufactures the Lilium a-200E, a device designed for transdermal drug delivery, likely targeting localized or systemic medication administration through the skin.
The company’s portfolio is regulated under Class II devices in the United States, with the Lilium a-200E listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the US.
Catalogue
Lilium a-200E Ref K170046
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lilium Otsuka Co., Ltd. have in the registry?
The registry currently lists 1 device for Lilium Otsuka Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lilium Otsuka Co., Ltd.'s devices?
Among its 1 most recently registered device, Lilium Otsuka Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Lilium Otsuka Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lilium Otsuka Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lilium Otsuka Co., Ltd. in the registry?
The most recently registered devices listed for Lilium Otsuka Co., Ltd. include Lilium a-200E.