Lenstec, Inc.
United StatesFDA applicant, unverified FDA FEI 3001659659
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Regimes: 510(k) Registry: 510(k)
Lenstec Intraocular Lens (IOL) Injection System Ref K060533
Regimes: 510(k) Registry: 510(k)Lenstec LC Injection system Ref K161776
Regimes: 510(k) Registry: 510(k)Lenstec Lc Injection System Ref K063802
Regimes: 510(k) Registry: 510(k)Lenstec Lc Injection System Ref K122848
Regimes: 510(k) Registry: 510(k)Fluid Isolation Device Ref K091915
Regimes: 510(k) Registry: 510(k)The Softec Hd IOL Ref P090022
Regimes: PMA Registry: PMAClearView 3 IOL Ref P200020
Regimes: PMA Registry: PMA
Company details
- FDA FEI number
- 3001659659
- Address
- 1765 Commerce Ave N, Saint Petersburg, FL, 33716
Frequently asked questions
How many devices does Lenstec, Inc. have in the registry?
The registry currently lists 8 devices for Lenstec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lenstec, Inc.'s devices?
Among its 8 most recently registered devices, Lenstec, Inc. has devices listed in FDA 510(k) (6 devices) and FDA PMA (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Lenstec, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Lenstec, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Lenstec, Inc. in the registry?
The most recently registered devices listed for Lenstec, Inc. include LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSES, LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM, Lenstec LC Injection system and FLUID ISOLATION DEVICE.