MedShape, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
MedShape, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DynaNail Mini, DynaNail TTC Fusion System, DynaNail Mini Tapered Hybrid
16
Total
16
Cleared
0
Denied
MedShape, Inc. has 16 FDA 510(k) cleared orthopedic devices. Based in Atlanta, US.
Latest FDA clearance: Mar 2026. Active since 2012.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - MedShape, Inc.
16 devices
Cleared
Mar 18, 2026
DynaNail Mini
Orthopedic
89d
Cleared
Sep 12, 2025
DynaNail TTC Fusion System
Orthopedic
193d
Cleared
Mar 21, 2024
DynaNail Mini Tapered Hybrid
Orthopedic
27d
Cleared
Aug 19, 2022
DynaClip® Bone Staple
Orthopedic
151d
Cleared
Jan 04, 2022
DynaFuse Fixation System
Orthopedic
391d
Cleared
Jan 15, 2021
Dynanail Mini Hybrid
Orthopedic
59d
Cleared
Apr 23, 2020
DynaClip Bone Staple
Orthopedic
146d
Cleared
Feb 14, 2019
DynaNail Mini
Orthopedic
141d
Cleared
Nov 05, 2018
DynaClipTM Bone Staple
Orthopedic
125d
Cleared
Nov 02, 2017
DynaNail TTC Fusion System
Orthopedic
176d
Cleared
Dec 18, 2014
FASTFORWARD
Orthopedic
203d
Cleared
Sep 29, 2014
HELICAL RIDGE PEEK INTERFERENCE SCREW
Orthopedic
133d