Sterilab, Inc.
United Statesfrom the FDA registration address FDA FEI 3016255836
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Sterilab, Inc. makes
Sterilab, Inc. manufactures medical devices including cannulas, cystotomes, needles, and lens manipulators.
The company's products are Class I devices listed in the FDA 510(k) registry, and Sterilab is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3016255836
- Address
- 1040 Morningside Drive, Naples, FL, 34103
Frequently asked questions
How many devices does Sterilab, Inc. have in the registry?
The registry currently lists 1 device for Sterilab, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterilab, Inc.'s devices?
Among its 1 most recently registered device, Sterilab, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sterilab, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sterilab, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sterilab, Inc. in the registry?
The most recently registered devices listed for Sterilab, Inc. include STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORS.