MedShape, Inc.
MedShape, Inc. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2026, with 2 FDA device recalls on record.
Top product codes for MedShape, Inc.
FDA recalls by MedShape, Inc.
- Z-2513-2025 — Medshape Universal Joints, REF: DNE-9000-UJ
- Z-0453-2022 — DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by MedShape, Inc.
- K254110 — DynaNail Mini; DynaNail Hybrid; DynaNail Helix; DynaClip; DynaClip Forte; DynaClip Delta; DynaClip Quattro
- K250628 — DynaNail TTC Fusion System
- K240530 — DynaNail Mini Tapered Hybrid
- K220812 — DynaClip® Bone Staple
- K203595 — DynaFuse Fixation System
- K203381 — Dynanail Mini Hybrid
- K193305 — DynaClip Bone Staple
- K182677 — DynaNail Mini
- K181781 — DynaClipTM Bone Staple
- K171376 — DynaNail TTC Fusion System
- K141420 — FASTFORWARD
- K141290 — HELICAL RIDGE PEEK INTERFERENCE SCREW
- K132783 — EXOSHAPE DUO SOFT TISSUE FASTENER
- K130467 — POROUS MORPHIX SUTURE ANCHOR WITH FORCE FIBER SUTURE
- K123350 — ECLIPSE SOFT TISSUE FASTENER
- K113828 — DYNANAIL ANKLE ARTHRODESIS NAIL
Data sourced from openFDA. This site is unofficial and independent of the FDA.