TroCare, LLC
United StatesFDA 510(k) applicant, unverified FDA FEI 3045813414
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What TroCare, LLC makes
TroCare, LLC manufactures the TroKit Laparoscope Lens Wiper, a disposable device designed to clean and maintain the optical clarity of laparoscopic lenses during surgical procedures.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
TroKit Laparoscope Lens Wiper Ref K253994
510(k) 510(k)TroCare TroKit Laparoscope Lens Wiper (CP000626) Ref K241796
510(k) 510(k)
Company details
- FDA FEI number
- 3045813414
- Address
- C/O Polsinelli, Houston, TX, 77002
Frequently asked questions
How many devices does TroCare, LLC have in the registry?
The registry currently lists 2 devices for TroCare, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list TroCare, LLC's devices?
Among its 2 most recently registered devices, TroCare, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do TroCare, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for TroCare, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TroCare, LLC in the registry?
The most recently registered devices listed for TroCare, LLC include TroKit Laparoscope Lens Wiper and TroCare TroKit Laparoscope Lens Wiper (CP000626).