Adicon
Country not established
- Devices
- 1
What Adicon makes
Adicon manufactures sterile, single-use operating room procedural packs designed for surgical and procedural applications. These packs include essential instruments, drapes, and supplies tailored for specific medical procedures to ensure sterile environments during surgery.
The company’s procedural packs are regulated under the FDA’s 510(k) clearance process as Class II devices. These products are listed in the U.S. market and comply with relevant FDA requirements for surgical and procedural use.
Catalogue
Operating Room Procedural Pack Ref K822804
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adicon have in the registry?
The registry currently lists 1 device for Adicon. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adicon's devices?
Among its 1 most recently registered device, Adicon has devices listed in FDA 510(k) (1 device).
What are the newest devices from Adicon in the registry?
The most recently registered devices listed for Adicon include OPERATING ROOM PROCEDURAL PACK.