Ximedica
Country not established
- Devices
- 2
What Ximedica makes
Ximedica manufactures ENDOCOLLECT Specimen Retrieval Bags in three sizes (8mm, 12mm, and 15mm) for collecting and preserving biopsy specimens during endoscopic procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
ENDOCOLLECT Specimen Retrieval Bag Ref K232519
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ximedica have in the registry?
The registry currently lists 2 devices for Ximedica. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ximedica's devices?
Among its 2 most recently registered devices, Ximedica has devices listed in FDA 510(k) (2 devices).
What risk classes do Ximedica's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ximedica's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ximedica in the registry?
The most recently registered devices listed for Ximedica include ENDOCOLLECT Specimen Retrieval Bag, 8mm, ENDOCOLLECT Specimen Retrieval Bag, 12mm, ENDOCOLLECT Specimen Retrieval Bag, 15mm and ENDOCOLLECT Specimen Retrieval Bag.