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Medshape, Inc.

Last updated September 17, 2026

Information

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

Catalogue (563)

Page 7 of 12

Device	Model / Reference	Registries	Class	Status
Ef1	DNE-9000-350-PTB	FDA UDI	Class II	Active
ExoShape	1101-00-0730	FDA UDI	Class II	Active
DynaNail	2201-06-0100	FDA UDI	Class I	Active
Ef1	DNE-160-C	FDA UDI	Class II	Active
ExoShape	1100-00-1130	FDA UDI	Class II	Active
Ef1	DNE-180-DXFP	FDA UDI	Class II	Active
DynaNail Helix, Headed, 90mm	3200-00-7090	FDA UDI	Class II	Active
DynaNail Hybrid	2601-00-7060	FDA UDI	Class II	Active
Ef1	F4-145180	FDA UDI	Class II	Active
DynaNail	2200-04-0140	FDA UDI	Class I	Active
Drill, variable size, DynaClip staple, 3.0mm	ED-10802.030	FDA UDI	Class I	Active
DynaNail Hybrid	2601-00-7070	FDA UDI	Class II	Active
DynaNail Helix, Headless, 75mm	3200-01-7075	FDA UDI	Class II	Active
DynaNail	1200-01-1022	FDA UDI	Class II	Active
DynaNail	1200-02-5050	FDA UDI	Class II	Active
DynaNail	2200-12-0035	FDA UDI	Class I	Active
DynaNail Helix, Headless, 55mm	3200-01-7055	FDA UDI	Class II	Active
DynaNail Hybrid	2601-00-7130	FDA UDI	Class II	Active
DynaNail Hybrid	2601-00-7120	FDA UDI	Class II	Active
Ef1	F4-134180	FDA UDI	Class II	Active
Ef1	DNE-00-RS	FDA UDI	Class II	Active
Ef1	DNE-518045	FDA UDI	Class II	Active
Ef1	DNE-6000-350	FDA UDI	Class II	Active
DynaNail Mini	2600-00-8100	FDA UDI	Class II	Active
Ef1	DNE-418045	FDA UDI	Class II	Active
Kitsune	2800-02-020	FDA UDI	Class I	Active
Ef1	DNE-3-MP	FDA UDI	Class II	Active
Joint Shim	3400-16-000	FDA UDI	Class I	Active
Eclipse	1500-00-0712	FDA UDI	Class II	Active
Ef1	14-1109-R0	FDA UDI	Class II	Active
Morphix XT	1000-10-035	FDA UDI	Class I	Active
Ef1	DNE-160-DRFP	FDA UDI	Class II	Active
Ef1	DNE-9000-TH-532	FDA UDI	Class I	Active
Ef1	DNE-6000-201	FDA UDI	Class II	Active
DynaNail	1200-02-5045	FDA UDI	Class II	Active
DynaNail Mini	2600-00-8110	FDA UDI	Class II	Active
DynaNail	1200-02-5060	FDA UDI	Class II	Active
Ef1	DNE-20-B	FDA UDI	Class II	Active
FastForward	1700-00-001	FDA UDI	Class II	Active
ExoShape Femoral	1600-00-011	FDA UDI	Class II	Active
Morphix XT	1000-04-235	FDA UDI	Class II	Unknown
Ef1	DNE-180-DHFP	FDA UDI	Class II	Active
Ef1	DNE-4-MP	FDA UDI	Class II	Active
Morphix	1000-03-345	FDA UDI	Class II	Active
DynaClip	3000-00-201818	FDA UDI	Class II	Active
Joint Finder Fulcrum, Left	3400-08-001	FDA UDI	Class I	Active
DynaNail	1200-02-5055	FDA UDI	Class II	Active
Ef1	DNE-140-5	FDA UDI	Class II	Active
Helical Ridge	2400-05-020	FDA UDI	Class I	Active
DynaNail Mini	2600-04-4338	FDA UDI	Class II	Active

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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.

Date	Recall No.	Class	Status	Reason
Jun 2, 2025	Z-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, 2021	Z-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.