Evermed, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 9
What Evermed, Inc. makes
Evermed, Inc. manufactures sterile and non-sterile medical devices, including injection caps for central venous catheters, tunneling instruments for catheter placement, peritoneal access catheters, and catheter repair kits. Their portfolio also includes non-sterile parenteral administration components and single/double lumen catheters.
These devices are classified under Class II in the U.S. regulatory framework and are listed via FDA 510(k) clearance. The company is based in the United States.
Catalogue
Explorer Powered Wheelchair Ref K023485
510(k) 510(k)Sterile Hichman/Broviac Injection Cap Ref K840846
510(k) 510(k)Steiger Tunneling Instrument 285 Ref K840529
510(k) 510(k)Galaxy Series Wheelchair Ref K023993
510(k) 510(k)Millennium Series Manual Wheelchairs Ref K024030
510(k) 510(k)Non-Sterile Peritoneal Access Cathet- Ref K830257
510(k) 510(k)Non-Sterile Catheter Repair Kits Ref K830406
510(k) 510(k)Non-Sterile Broviac Parenteral Alimi- Ref K830256
510(k) 510(k)Non-Sterile, Single/Souble Lumen-Cath Ref K830233
510(k) 510(k)
Frequently asked questions
How many devices does Evermed, Inc. have in the registry?
The registry currently lists 9 devices for Evermed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Evermed, Inc.'s devices?
Among its 9 most recently registered devices, Evermed, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Evermed, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Evermed, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Evermed, Inc. in the registry?
The most recently registered devices listed for Evermed, Inc. include EXPLORER POWERED WHEELCHAIR, STERILE HICHMAN/BROVIAC INJECTION CAP, STEIGER TUNNELING INSTRUMENT 285 and GALAXY SERIES WHEELCHAIR.