MedShape, Inc. is one of 26109 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 Helix® Fixation System, DynaNail Mini, DynaNail TTC Fusion System
17
Total
17
Cleared
0
Denied
MedShape, Inc. has 17 FDA 510(k) cleared orthopedic devices. Based in Atlanta, US.
Latest FDA clearance: Sep 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.
17 devices
Cleared
Sep 23, 2026
DynaNail Helix® Fixation System
Orthopedic
181d
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
Cleared
Dec 09, 2013
EXOSHAPE DUO SOFT TISSUE FASTENER
Orthopedic
94d
Cleared
Dec 05, 2013
POROUS MORPHIX SUTURE ANCHOR WITH FORCE FIBER SUTURE
Orthopedic
283d
Cleared
Mar 07, 2013
ECLIPSE SOFT TISSUE FASTENER
Orthopedic
127d
Cleared
Feb 29, 2012
DYNANAIL ANKLE ARTHRODESIS NAIL
Orthopedic
64d