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ATLAS SPINE INC.

US

Last updated September 17, 2026

Information

Country
US
Address
1555 Jupiter Park Dr Ste 1, JUPITER, FL, 33458
Website
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LinkedIn
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Facebook
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Email
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Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3003855635
DUNS Number
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Catalogue (910)

Page 10 of 19
DeviceModel / ReferenceRegistriesClassStatus
Apelo® / Apelo® MIS 1110-03-5545
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1110-02-4530
FDA UDI
Class IIActive
HiJAK™ Stand Alone 1123-02-0007
FDA UDI
Class IIActive
V3™ Segmental Plating System 1121-03-0016
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1106-01-4545
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 2010-78-0000
FDA UDI
Class IActive
Stature® STL-013-010
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 6900-13-0550
FDA UDI
Class IIActive
Verteview® VSA-100-038
FDA UDI
Class IIActive
HiJAK™ Cervical 1119-01-0014
FDA UDI
Class IIActive
Stature® STL-017-014
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 6006-06-0000
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 2010-16-0750
FDA UDI
Class IActive
Apelo® / Apelo® MIS 1100-08-0050
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1106-03-6535
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 6006-02-0000
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1100-10-0095
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1106-02-8555
FDA UDI
Class IIActive
HiJAK™ Stand Alone 1123-02-0009
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1106-09-0000
FDA UDI
Class IIActive
Verteview® VSS-042-012
FDA UDI
Class IIActive
Stature® STL-011-008
FDA UDI
Class IIActive
Verteview® VSA-400-092
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
HiJAK™ Cervical 1119-09-0009
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
V3” Segmental Plating System 1121-05-0011
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1106-02-6540
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1100-16-0065
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1100-10-0105
FDA UDI
Class IIActive
HiJAK™ Cervical 2019-04-0010
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1100-16-0045
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1110-02-7550
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1110-01-7530
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1110-01-7560
FDA UDI
Class IIActive
HiJAK™ Cervical 1119-01-0010
FDA UDI
Class IIActive
Rebar® SCC-002-006
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1106-01-5530
FDA UDI
Class IIActive
V3” Segmental Plating System 1121-05-0008
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 1100-14-0105
FDA UDI
Class IIActive
Apelo® / Apelo® MIS 2010-08-0000
FDA UDI
Class IActive
Apelo® / Apelo® MIS 1100-03-0055
FDA UDI
Class IIActive
HiJAK™ Stand Alone 1123-02-0012
FDA UDI
Class IIActive
True Position® True Position®
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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Importers

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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.

DateRecall No.ClassStatusReason
Jul 26, 2013Z-1616-2016—terminated

The device was not appropriately set to mitigate the risk of implant fracture upon rotation inside the disc space.

Jun 4, 2009Z-2274-2012—terminated

Atlas Spine, Inc. recalled their Apelo Modular Screwdriver, a component of the Apelo Pedicle Screw System Instrumentation, because of complaints received about the tip breaking. If the tip is fractured inside of the modular screw, the tip could become implanted in the body or if the entire screw is removed, it could cause a delay in the surgery.