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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 9 of 12

Device	Model / Reference	Registries	Class	Status
DynaNail	1200-03-5100	FDA UDI	Class II	Active
Ef1	DNE-9010-100S	FDA UDI	Class I	Active
Ef1	DNE-418025	FDA UDI	Class II	Active
DynaNail	2200-05-0070	FDA UDI	Class I	Active
Ef1	DNE-120-OV	FDA UDI	Class II	Active
DynaNail Helix, Headless, 90mm	3200-01-7090	FDA UDI	Class II	Active
Ef1	DNE-240-SFC	FDA UDI	Class II	Active
Acorn Reamer, 10mm	2300-01-100	FDA UDI	Class I	Active
DynaNail Mini	2900-24-0250	FDA UDI	Class I	Active
Trajectory Wire, DynaFuse	3100-04-0001	FDA UDI	Class I	Active
DynaClip Quattro	3000-11-221616	FDA UDI	Class II	Active
DynaClip	3000-03-026	FDA UDI	Class I	Active
Ef1	DNE-200-DRFP	FDA UDI	Class II	Active
ExoShape	1101-00-1230	FDA UDI	Class II	Active
Ef1	DNE-9000-AD-003	FDA UDI	Class I	Active
Ef1	DNE-200-DHFP	FDA UDI	Class II	Active
Ef1	DNE-140-OV	FDA UDI	Class II	Active
Ef1	DNE-6000-100S	FDA UDI	Class II	Active
DynaNail Helix, Headed, 105mm	3200-00-7105	FDA UDI	Class II	Active
Ef1	DNE-9000-500-PTB	FDA UDI	Class II	Active
DynaNail	1200-03-5065	FDA UDI	Class II	Active
Kitsune	2800-01-000	FDA UDI	Class I	Active
Driver Guide, Helical Ridge	2400-01-000	FDA UDI	Class I	Active
Ef1	DNE-140-SFC	FDA UDI	Class II	Active
DynaNail	1200-04-0000	FDA UDI	Class II	Active
Helical Ridge	1400-15-0475	FDA UDI	Class II	Active
Ef1	DNE-180-DRFP	FDA UDI	Class II	Active
Ef1	DNE-180-5	FDA UDI	Class II	Active
Pin, 3.0mm, DynaClip Staple, 3.0mm	ED-10801-030	FDA UDI	Class II	Active
Ef1	DNE-9000-250-CF	FDA UDI	Class II	Active
DynaNail Mini	2600-04-4326	FDA UDI	Class II	Active
Ef1	DNE-3-FP	FDA UDI	Class II	Active
DynaNail Mini	2600-03-4314	FDA UDI	Class II	Active
Drill, variable size, wolverine, DynaClip staple, 2.0mm	ED-10877-020	FDA UDI	Class I	Active
Acorn Reamer, 6.5mm	2300-01-065	FDA UDI	Class I	Active
Ef1	DNE-140-SFU	FDA UDI	Class II	Active
DynaNail Mini	2900-16-055	FDA UDI	Class I	Active
Ef1	DNE-418035	FDA UDI	Class II	Active
Ef1	DNE-4000-300	FDA UDI	Class II	Active
DynaNail	1200-02-5027	FDA UDI	Class II	Active
Depth Gauge, 150mm DynaFuse	3100-05-0150	FDA UDI	Class I	Active
DynaNail Mini	2900-21-0001	FDA UDI	Class I	Active
DynaClip Delta	3000-12-000	FDA UDI	Class I	Active
DynaNail Mini	2900-20-0000	FDA UDI	Class I	Active
Ef1	DNE-220-C	FDA UDI	Class II	Active
Drill, variable size, DynaClip staple, 2.0mm	ED-10802.020	FDA UDI	Class I	Active
DynaNail	1200-01-1222	FDA UDI	Class II	Active
DynaNail	2201-06-0130	FDA UDI	Class I	Active
DynaNail Mini	2600-00-7060	FDA UDI	Class II	Active
Ef1	DNE-9010-200L	FDA UDI	Class I	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.