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 5 of 12

Device	Model / Reference	Registries	Class	Status
DynaNail Mini	2600-00-8080	FDA UDI	Class II	Active
DynaNail Mini	2600-00-8090	FDA UDI	Class II	Active
Eclipse	1500-01-055	FDA UDI	Class I	Active
Ef1	DNE-1000-015	FDA UDI	Class II	Active
Morphix	1000-03-255	FDA UDI	Class II	Active
Ef1	DNE-3-PL	FDA UDI	Class II	Active
Ef1	DNE-160-OV	FDA UDI	Class II	Active
Ef1	DNE-50-150	FDA UDI	Class I	Active
FastForward	1700-00-002	FDA UDI	Class II	Active
Ef1	DNE-240-SFU	FDA UDI	Class II	Active
DynaNail Helix, Headless, 100mm	3200-01-7100	FDA UDI	Class II	Active
Eclipse	1500-00-0612	FDA UDI	Class II	Active
Kitsune	2800-02-008	FDA UDI	Class I	Active
Kitsune	2800-04-020	FDA UDI	Class I	Active
Ef1	DNE-25-TR	FDA UDI	Class II	Active
Ef1	DNE-1000-WFB	FDA UDI	Class II	Active
Knurled Driver Attachment, Helical Ridge	2400-06-000	FDA UDI	Class I	Active
Eclipse	1500-00-0417	FDA UDI	Class II	Active
DynaNail Mini	2600-00-7080	FDA UDI	Class II	Active
Ef1	DNE-9000-450-PTB	FDA UDI	Class II	Active
Ef1	DNE-9000-TH-964L	FDA UDI	Class I	Active
Ef1	DNE-120-TR	FDA UDI	Class II	Active
Ef1	DNE-9000-AD-006	FDA UDI	Class I	Active
Eclipse	1500-00-0620	FDA UDI	Class II	Active
Ef1	DNE-9000-BACC	FDA UDI	Class II	Active
DynaNail Mini	2600-00-8070	FDA UDI	Class II	Active
ExoShape Teno	1100-01-0720	FDA UDI	Class II	Active
DynaNail Helix, Headed, 95mm	3200-00-7095	FDA UDI	Class II	Active
Ef1	DNE-9000-AD-005	FDA UDI	Class I	Active
DynaNail Mini	2900-02-0400	FDA UDI	Class I	Active
DynaNail	2200-04-0633	FDA UDI	Class I	Active
Eclipse	1500-01-070	FDA UDI	Class I	Active
DynaNail	2200-12-0135	FDA UDI	Class I	Active
DynaNail Mini	2600-00-7140	FDA UDI	Class II	Active
DynaNail	2201-09-0025	FDA UDI	Class I	Active
DynaNail Helix, Headless, 105mm	3200-01-7105	FDA UDI	Class II	Active
DynaNail	2200-09-0040	FDA UDI	Class I	Active
ExoShape	1101-00-0830	FDA UDI	Class II	Active
Ef1	DNE-6000-150	FDA UDI	Class II	Active
DynaNail Mini	2600-00-7130	FDA UDI	Class II	Active
Ratcheting Handle, Mini AO and ZSI-Hall Combo, DynaFuse	3100-10-0001	FDA UDI	Class I	Active
DynaNail Mini	2600-03-4318	FDA UDI	Class II	Active
DynaNail Hybrid	2601-00-7080	FDA UDI	Class II	Active
Eclipse	2300-01-050	FDA UDI	Class I	Active
FastForward	1700-00-000	FDA UDI	Class II	Active
DynaNail	1200-03-5070	FDA UDI	Class II	Active
Tube Caddy, DynaFuse	3100-12-0001	FDA UDI	Class II	Active
Ef1	DNE-220-DHFP	FDA UDI	Class II	Active
DynaClip Quattro	3000-11-222020	FDA UDI	Class II	Active
ExoShape	1100-00-1130	FDA UDI	Class II	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.