Std Mfg., Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Std Mfg., Inc. makes
Std Mfg., Inc. manufactures vascular closure devices, including systems combining suction and stapling for sealing blood vessels, as well as resurfacing systems for the femoral and humeral joints. Their portfolio also includes an irrigation pump designed for surgical use.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are based in the United States.
Catalogue
Vascular Closure Device Ref K003169
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Modification To Vascular Closure Device Ref K012362
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Std Irrigation Pump Ref K930427
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Std Mfg., Inc. have in the registry?
The registry currently lists 6 devices for Std Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Std Mfg., Inc.'s devices?
Among its 6 most recently registered devices, Std Mfg., Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Std Mfg., Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Std Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Std Mfg., Inc. in the registry?
The most recently registered devices listed for Std Mfg., Inc. include VASCULAR CLOSURE DEVICE, SUCTION VASCULAR STAPLER AND IMPLANTABLE STAPLE SYSTEM, CONTOURED ARTICULAR PROSTHESIS (CAP) FEMORAL HEAD RESURFACING SYSTEM and MODIFICATION TO VASCULAR CLOSURE DEVICE.