TroCare, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
TroCare, LLC - FDA 510(k) Cleared Devices
Recent clearances: TroKit Laparoscope Lens Wiper, TroCare TroKit Laparoscope Lens Wiper (CP000626)
2
Total
2
Cleared
0
Denied
TroCare, LLC has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by TroCare, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by QSR Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - TroCare, LLC
2 devices