Avanca Medical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Avanca Medical Devices, Inc. makes
Avanca Medical Devices, Inc. manufactures procedural safety syringe devices, including the Procedur SF Safety Syringe Device and the Procedur-10, designed to enhance safety during injections and fluid administration by preventing accidental needle sticks and contamination.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Procedur Sf Safety Syringe Device Ref K042487
Regimes: 510(k) Registry: 510(k)Procedur-10 Ref K052075
Regimes: 510(k) Registry: 510(k)Procedur 10 Syringe Device Ref K042486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Avanca Medical Devices, Inc. have in the registry?
The registry currently lists 3 devices for Avanca Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avanca Medical Devices, Inc.'s devices?
Among its 3 most recently registered devices, Avanca Medical Devices, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Avanca Medical Devices, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Avanca Medical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avanca Medical Devices, Inc. in the registry?
The most recently registered devices listed for Avanca Medical Devices, Inc. include PROCEDUR SF SAFETY SYRINGE DEVICE, PROCEDUR-10 and PROCEDUR 10 SYRINGE DEVICE.