Paragon Implant Mfg., LLC is one of 16099 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paragon Implant Mfg., LLC - FDA 510(k) Cleared Devices
Recent clearances: TriActive Dental Implant System, NizPlant Dental Implant System, GEN5™ and GEN5+™ 3.3mmD Dental Implants
5
Total
5
Cleared
0
Denied
Paragon Implant Mfg., LLC has 5 FDA 510(k) cleared medical devices. Based in Calabasas, US.
Latest FDA clearance: Sep 2026. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Paragon Implant Mfg., LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Paragon Implant Mfg., LLC
5 devices
Cleared
Sep 17, 2026
TriActive Dental Implant System
Dental
141d
Cleared
Dec 23, 2025
NizPlant Dental Implant System
Dental
307d
Cleared
Dec 23, 2025
GEN5™ and GEN5+™ 3.3mmD Dental Implants
Dental
167d
Cleared
Nov 14, 2025
Sterilization Trays
General Hospital
158d
Cleared
Oct 30, 2025
GEN5 and GEN5+ Dental Implant System
Dental
128d