Is this your brand? Sign in to claim ownership.

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 4 of 12

Device	Model / Reference	Registries	Class	Status
Ef1	DNE-4-FP	FDA UDI	Class II	Active
DynaNail	2201-09-0040	FDA UDI	Class I	Active
Ef1	DNE-6000-500	FDA UDI	Class II	Active
Ratcheting, Petite AO Quick Connect Handle	3400-12-000	FDA UDI	Class I	Active
DynaNail Hybrid	2901-00-0078	FDA UDI	Class I	Active
DynaNail	1200-01-1026	FDA UDI	Class II	Active
Ef1	DNE-1000-OE	FDA UDI	Class I	Active
Ef1	DNE-120-DXFP	FDA UDI	Class II	Active
Ef1	DNE-9000-PLY	FDA UDI	Class I	Active
Eclipse	1500-00-0512	FDA UDI	Class II	Active
Morphix	1000-03-355	FDA UDI	Class II	Active
Morphix XT	1000-10-025	FDA UDI	Class I	Active
Ef1	6206-0002000-00	FDA UDI	Class I	Active
DynaNail Mini	2900-01-0200	FDA UDI	Class I	Active
DynaNail Helix, Washer, 15 mm	3300-00-1515	FDA UDI	Class II	Active
Ef1	DNE-9000-DACC	FDA UDI	Class II	Active
Ef1	DNE-9000-TE	FDA UDI	Class I	Active
Ef1	1499-000-002	FDA UDI	Class I	Active
Double-Ended Lateral Retractor	3400-17-000	FDA UDI	Class I	Active
DynaNail Mini	2900-04-0229	FDA UDI	Class I	Active
DynaNail Mini	2600-00-8140	FDA UDI	Class II	Active
Eclipse	1500-02-000	FDA UDI	Class I	Active
Morphix XT	1000-10-045	FDA UDI	Class I	Active
Ef1	DNE-9000-TH-964	FDA UDI	Class I	Active
Ef1	DNE-618025	FDA UDI	Class II	Active
Ef1	DNE-5-MP	FDA UDI	Class II	Active
Ef1	DNE-80-TR	FDA UDI	Class II	Active
DynaNail	2200-24-0003	FDA UDI	Class I	Active
Ef1	DNE-9000-350-CF	FDA UDI	Class II	Active
DynaClip	3000-03-018	FDA UDI	Class I	Active
Dynanail Mini	2900-16-075	FDA UDI	Class I	Active
DynaClip	3000-02-002	FDA UDI	Class I	Active
DynaNail	1200-03-5085	FDA UDI	Class II	Active
Ef1	DNE-40-150	FDA UDI	Class I	Active
Ef1	DNE-140-DHFP	FDA UDI	Class II	Active
Ef1	DNE-180-34	FDA UDI	Class II	Active
Ef1	DNE-6000-033	FDA UDI	Class II	Active
Cannulated Drill, 4.0MM	2300-02-040	FDA UDI	Class I	Active
ExoShape	1100-00-0930	FDA UDI	Class II	Active
Ef1	DNE-518025	FDA UDI	Class II	Active
DynaNail	1200-03-5095	FDA UDI	Class II	Active
Clamp T Handle (Black) Short with 5/32 tool shaft	DNE-9000-TH-532S	FDA UDI	Class II	Active
DynaClip	3000-00-080808	FDA UDI	Class II	Active
Ef1	DNE-6000-750	FDA UDI	Class II	Active
DynaNail Mini	2900-01-0300	FDA UDI	Class I	Active
ExoShape	1100-00-0830	FDA UDI	Class II	Active
DynaNail	1200-03-5110	FDA UDI	Class II	Active
Ef1	752-000-001	FDA UDI	Class I	Active
Kitsune	2800-02-025	FDA UDI	Class I	Active
DynaNail	2201-06-0135	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.