Ipax, Inc.
United StatesFDA applicant, unverified FDA FEI 1720734
- Devices
- 18
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Ipax, Inc. makes
Ipax, Inc. manufactures ophthalmic and surgical devices including external eyelid weights (such as the Blink External Eyelid Weight and Blink Gold Eyelid Weight series), ophthalmic filter micro capsules, venipuncture systems (including the Timeline Venipuncture System and TIMLEINE(TM) Venipuncture System), sterile tube sets (ProntoPump Sterile Tube Set), surgical system components (KPE Plus-Pak Surgical System, I/A/KPE Tip, KPE 220 TS nonsterile), and related assembly parts such as Catalog No. I/A 100 and KPE 200 and procedural changes for Plus Paks.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Ipax, Inc. is based in the United States.
Catalogue
Search and filter all 18 devicesCompany details
- FDA FEI number
- 1720734
- Address
- 2700 S Raritan St, Englewood, CO, 80110
Frequently asked questions
How many devices does Ipax, Inc. have in the registry?
The registry currently lists 18 devices for Ipax, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ipax, Inc.'s devices?
Among its 18 most recently registered devices, Ipax, Inc. has devices listed in FDA 510(k) (18 devices).
What risk classes do Ipax, Inc.'s devices fall under?
Among its 18 most recently registered devices, the classes recorded for Ipax, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ipax, Inc. in the registry?
The most recently registered devices listed for Ipax, Inc. include BLINK EXTERNAL EYELID WEIGHT, TIMELINE VENIPUNCTURE SYSTEM, OPHTHALMIC FITLER MICRO CAPSULE and ProntoPump Sterile Tube Set.