Engineering, Inc.
Also registered as Kg Engineering, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
LS9000 Suction Biopsy Needle Ref K862749
Regimes: 510(k) Registry: 510(k)LS3000 Cannula Uterine Suction Ref K862476
Regimes: 510(k) Registry: 510(k)LS1000 Surgical Aspirator Ii Ref K854844
Regimes: 510(k) Registry: 510(k)Combo 36 Ref K854257
Regimes: 510(k) Registry: 510(k)Modified Servo Syringe Ref K881521
Regimes: 510(k) Registry: 510(k)Auto Entry System (Mate) Ref K870425
Regimes: 510(k) Registry: 510(k)LM2000A Surgical Suction Monitor Ref K854359
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Engineering, Inc. have in the registry?
The registry currently lists 7 devices for Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Engineering, Inc.'s devices?
Among its 7 most recently registered devices, Engineering, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Engineering, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Engineering, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Engineering, Inc. in the registry?
The most recently registered devices listed for Engineering, Inc. include LS9000 SUCTION BIOPSY NEEDLE, LS3000 CANNULA UTERINE SUCTION, LS1000 SURGICAL ASPIRATOR II and COMBO 36.