TriMed, Inc. is one of 12957 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
TriMed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Large Compression Screws, TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD), TriMed Compression Screws
38
Total
38
Cleared
0
Denied
TriMed, Inc. has 38 FDA 510(k) cleared orthopedic devices. Based in Saugus, US.
Latest FDA clearance: Aug 2026. Active since 2005.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tech2med, LLC, Jean Asquith and Tech2med. 3 submissions have an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - TriMed, Inc.
38 devices
Cleared
Aug 12, 2026
Large Compression Screws
Orthopedic
33d
Cleared
Jul 16, 2026
TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD)
Orthopedic
29d
Cleared
May 14, 2026
TriMed Compression Screws
Orthopedic
29d
Cleared
Jan 15, 2026
TriMed Volar Bearing Plates (VBEAL-13-7S)
Orthopedic
31d
Cleared
Aug 20, 2025
Distal Xtremities System
Orthopedic
50d
Cleared
Jul 11, 2025
RipCord
Orthopedic
91d
Cleared
Jul 10, 2025
TriMed Total Wrist Fusion System (Total Wrist Fusion Plate)
Orthopedic
15d
Cleared
Jun 26, 2025
TriMed Ulnar Osteotomy System (Ulnar Osteotomy Compression Plate)
Orthopedic
90d
Cleared
May 22, 2025
TriMed Fifth Metatarsal System (Fifth Metatarsal Plate)
Orthopedic
55d
Cleared
Apr 10, 2025
TriMed® Compression Screws
Orthopedic
111d
Cleared
Apr 08, 2025
TriMed Fusion Cup System
Orthopedic
18d
Cleared
Mar 19, 2025
TriMed Elbow and Forearm System
Orthopedic
86d
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