Injectimed, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Injectimed, Inc. makes
Injectimed, Inc. manufactures medical devices including the Frontline Medical SafetyNet Guidewire Introducer, a catheter-based introducer designed for vascular procedures, and the SafetyNet Guidewire Introducer, a similar device for guiding wires in interventional radiology. The company also produces the Protector Syringe Safety Cap System, a protective cap for syringes to prevent needle sticks and contamination during use.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with several products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Frontline Medical Safetynet Guidewire Introducer Ref K073664
Regimes: 510(k) Registry: 510(k)Safetynet Guidewire Introducer Ref K040029
Regimes: 510(k) Registry: 510(k)Protector Syringe Safety Cap System Ref K922158
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Injectimed, Inc. have in the registry?
The registry currently lists 3 devices for Injectimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Injectimed, Inc.'s devices?
Among its 3 most recently registered devices, Injectimed, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Injectimed, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Injectimed, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Injectimed, Inc. in the registry?
The most recently registered devices listed for Injectimed, Inc. include FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCER, SAFETYNET GUIDEWIRE INTRODUCER and PROTECTOR SYRINGE SAFETY CAP SYSTEM.