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Medshape, Inc.

US

Last updated September 17, 2026

Information

Country
US
Address
1575 NORTHSIDE DR NW STE 440, Atlanta, GA, 30318
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3007593722
DUNS Number
601306413

Catalogue (563)

Page 6 of 12
DeviceModel / ReferenceRegistriesClassStatus
Ef1 DNE-9000-ACC
FDA UDI
Class IIActive
DynaClip Forte 3000-02-001
FDA UDI
Class IActive
DynaNail Mini 2900-05-0003
FDA UDI
Class IActive
Ef1 DNE-120-5
FDA UDI
Class IIActive
Eclipse 1500-00-0820
FDA UDI
Class IIActive
DynaNail Hybrid 2601-00-7110
FDA UDI
Class IIActive
Ef1 DNE-200-SFC
FDA UDI
Class IIActive
Ef1 DNE-9000-FW
FDA UDI
Class IIActive
Eclipse 1500-01-040
FDA UDI
Class IActive
Ef1 DNE-9000-TH-964S
FDA UDI
Class IActive
Ef1 DNE-160-SFC
FDA UDI
Class IIActive
DynaNail Hybrid 2601-00-7140
FDA UDI
Class IIActive
Eclipse 1500-00-0915
FDA UDI
Class IIActive
DynaNail Mini 2600-04-4330
FDA UDI
Class IIActive
DynaNail Mini 2600-00-8130
FDA UDI
Class IIActive
Kitsune 2800-03-020
FDA UDI
Class IActive
Evolve34 3400-20-000
FDA UDI
Class IActive
DynaClip 3000-03-010
FDA UDI
Class IActive
Eclipse 1500-00-0720
FDA UDI
Class IIActive
DynaNail Mini 2900-05-0004
FDA UDI
Class IActive
Ef1 DNE-200-DXFP
FDA UDI
Class IIActive
Counter Torque Wrench, Dynafuse 3100-06-0001
FDA UDI
Class IActive
Guide Pin, Surgibit Tip 2.4mm Diameter 1300-03-024
FDA UDI
Class IIActive
Helical Ridge 1400-20-0475
FDA UDI
Class IIActive
DynaNail 2201-06-0125
FDA UDI
Class IActive
Tap, Quick Connect, Reusable, Helical Ridge 2400-03-000
FDA UDI
Class IIActive
Item Master, Guide Pin, 2.4mm, Trocar Tip, 9in 1300-05-024
FDA UDI
Class IIActive
Morphix XT 1000-03-225
FDA UDI
Class IIActive
Ef1 DNE-220-DXFP
FDA UDI
Class IIActive
DynaNail 1200-03-5080
FDA UDI
Class IIActive
DynaNail Hybrid 2901-01-0075
FDA UDI
Class IActive
Ef1 DNE-200-34
FDA UDI
Class IIActive
DynaNail 2200-08-0080
FDA UDI
Class IActive
DynaNail 2201-06-0115
FDA UDI
Class IActive
Eclipse 1500-01-045
FDA UDI
Class IActive
DynaClip 3000-05-020
FDA UDI
Class IActive
DynaNail 1200-02-5022
FDA UDI
Class IIActive
T15 Driver, DynaNail Mini Hybrid 2901-02-0015
FDA UDI
Class IActive
Ef1 DNE-120-34
FDA UDI
Class IIActive
Ef1 DNE-6012-019A
FDA UDI
Class IIActive
Ef1 DNE-9000-AD-004
FDA UDI
Class IActive
DynaNail Helix, Headless, 80mm 3200-01-7080
FDA UDI
Class IIActive
Reusable Drill Guide Assembly, T-Shape, DynaClip, 12mm 3000-05-012
FDA UDI
Class IActive
Morphix XT 1000-03-235
FDA UDI
Class IIActive
DynaClip 3000-03-012
FDA UDI
Class IActive
DynaNail Helix, Headless, 85mm 3200-01-7085
FDA UDI
Class IIActive
Ef1 DNE-310025
FDA UDI
Class IIActive
DynaNail Mini 2900-16-050
FDA UDI
Class IActive
DynaNail Helix, Headless, 65mm 3200-01-7065
FDA UDI
Class IIActive
Ef1 DNE-518035
FDA UDI
Class IIActive

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Authorities

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FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Jun 2, 2025Z-2513-2025—open, classified

Bone external fixation system may have the pin that can become dislodged resulting in frame instability, the use of this product may cause a delay in surgery or a revision if the device is use.

Nov 17, 2021Z-0453-2022—open, classified

The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure.