Promed Advance Technology Co., Ltd.
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- Devices
- 1
What Promed Advance Technology Co., Ltd. makes
Promed Advance Technology Co., Ltd. manufactures OSTEO-LINK bone void filler pellets, a resorbable material designed to fill and support bone defects during surgical procedures.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Osteo-Link Bone Void Filler Pellets Ref K060809
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promed Advance Technology Co., Ltd. have in the registry?
The registry currently lists 1 device for Promed Advance Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promed Advance Technology Co., Ltd.'s devices?
Among its 1 most recently registered device, Promed Advance Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Promed Advance Technology Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Promed Advance Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promed Advance Technology Co., Ltd. in the registry?
The most recently registered devices listed for Promed Advance Technology Co., Ltd. include OSTEO-LINK BONE VOID FILLER PELLETS.