Ispg, Inc.
United StatesFDA applicant, unverified FDA FEI 1221435
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Ispg, Inc. makes
Ispg, Inc. manufactures single-use medical syringes and needles, including glass syringes, hypodermic syringe pistons, and Chiba needles, as well as anesthesia conduction needles for procedural and injection applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Anesthesia Conduction Needle Ref K962886
Regimes: 510(k) Registry: 510(k)Glass Syringe Ref K962042
Regimes: 510(k) Registry: 510(k)Hypodermic Syringe Piston Ref K950133
Regimes: 510(k) Registry: 510(k)Chiba Needle Ref K012358
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1221435
- Address
- 10504 Technology Ter, Lakewood Ranch, FL, 34211
Frequently asked questions
How many devices does Ispg, Inc. have in the registry?
The registry currently lists 4 devices for Ispg, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ispg, Inc.'s devices?
Among its 4 most recently registered devices, Ispg, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Ispg, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Ispg, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ispg, Inc. in the registry?
The most recently registered devices listed for Ispg, Inc. include ANESTHESIA CONDUCTION NEEDLE, GLASS SYRINGE, HYPODERMIC SYRINGE PISTON and CHIBA NEEDLE.