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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: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3007593722
DUNS Number: 601306413

Catalogue (563)

Page 2 of 12

Device	Model / Reference	Registries	Class	Status
ExoShape	1100-00-0628	FDA UDI	Class II	Active
DynaNail Mini	2600-05-0000	FDA UDI	Class II	Active
DynaClip	3000-00-181818	FDA UDI	Class II	Active
Kitsune	2800-04-015	FDA UDI	Class I	Active
DynaClip	3000-05-014	FDA UDI	Class I	Active
DynaNail Helix, Headed, 50mm	3200-00-7050	FDA UDI	Class II	Active
Ef1	DNE-6000-100XL	FDA UDI	Class II	Active
Ef1	DNE-9000-TH-AO	FDA UDI	Class I	Active
Ef1	DNE-6000-037	FDA UDI	Class II	Active
DynaNail	1200-03-5060	FDA UDI	Class II	Active
Eclipse	1500-04-0000	FDA UDI	Class I	Active
DynaNail	2200-15-0000	FDA UDI	Class I	Active
DynaNail Mini	2900-17-0000	FDA UDI	Class I	Active
Ef1	DNE-120-C	FDA UDI	Class II	Active
Ef1	DNE-9000-BTB	FDA UDI	Class II	Active
DynaNail Helix, Headless, 70mm	3200-01-7070	FDA UDI	Class II	Active
DynaNail Mini	2600-00-8060	FDA UDI	Class II	Active
DynaNail Mini	2600-04-4328	FDA UDI	Class II	Active
Eclipse	2300-01-090	FDA UDI	Class I	Active
DynaNail	2200-29-0000	FDA UDI	Class I	Active
DynaNail	1200-03-5090	FDA UDI	Class II	Active
Eclipse	1500-00-0520	FDA UDI	Class II	Active
Ef1	DNE-9000-BTC	FDA UDI	Class II	Active
Ef1	DNE-5000-300	FDA UDI	Class II	Active
ExoShape	1101-00-1030	FDA UDI	Class II	Active
DynaNail	2201-06-0120	FDA UDI	Class I	Active
DynaNail	2201-06-0105	FDA UDI	Class I	Active
Ef1	DNE-140-C	FDA UDI	Class II	Active
Cannulated Drill, 4.5MM	2300-02-045	FDA UDI	Class I	Active
DynaNail Mini	2600-00-7120	FDA UDI	Class II	Active
DynaNail Mini	2900-15-0002	FDA UDI	Class I	Active
Kitsune	2800-02-012	FDA UDI	Class I	Active
Ef1	DNE-300-TR	FDA UDI	Class II	Active
DynaClip Quattro	3000-09-022	FDA UDI	Class I	Active
Morphix XT	1000-04-125	FDA UDI	Class II	Active
DynaNail	2200-04-0033	FDA UDI	Class I	Active
Ef1	DNE-618045	FDA UDI	Class II	Active
DynaNail	2200-24-0002	FDA UDI	Class I	Active
DynaNail Mini	2600-04-4340	FDA UDI	Class II	Active
DynaFuse 5mm Drill	3100-01-0005	FDA UDI	Class I	Active
Ef1	DNE-2-FP	FDA UDI	Class II	Active
DynaNail Mini	2900-23-0000	FDA UDI	Class I	Active
DynaNail Mini	2900-21-0000	FDA UDI	Class I	Active
DynaClip Delta	3000-10-24161412	FDA UDI	Class II	Active
DynaNail	2200-18-5031	FDA UDI	Class I	Active
DynaNail Mini	2900-18-0000	FDA UDI	Class I	Active
Ef1	DNE-160-SFU	FDA UDI	Class II	Active
DynaNail Mini	2600-04-4324	FDA UDI	Class II	Active
Eclipse	1500-01-090	FDA UDI	Class I	Active
Ef1	DNE-9000-400-PTB	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.