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ATLAS SPINE INC.

Last updated September 17, 2026

Information

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

Catalogue (910)

Page 16 of 19

Device	Model / Reference	Registries	Class	Status
Apelo® / Apelo® MIS	1100-16-0030	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-02-0012	FDA UDI	Class II	Active
V3” Segmental Plating System	1121-05-0012	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-03-0065	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-06-0009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-4525	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-6560	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-13-0725	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1110-03-5525	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0003	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-10-0000	FDA UDI	Class II	Active
Rebar®	SCC-002-012	FDA UDI	Class II	Active
V3” Segmental Plating System	1121-05-0013	FDA UDI	Class II	Active
Verteview®	VSA-300-069	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-08-0013	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-8560	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-6535	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-8550	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-10-0075	FDA UDI	Class II	Active
Verteview®	VSA-300-063	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6006-04-0000	FDA UDI	Class II	Active
Rebar®	SCC-001-009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-02-7545	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-02-0009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0105	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-4525	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-6560	FDA UDI	Class II	Active
V3™ Segmental Plating System	1121-03-0012	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-4545	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-5525	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-48-0000	FDA UDI	Class I	Active
HiJAK™ Cervical	2019-05-0013	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-10-0090	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-08-0040	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-5525	FDA UDI	Class II	Active
Verteview®	VSA-400-080	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-5525	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-04-0008	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-07-0010	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-66-0000	FDA UDI	Class I	Active
Rebar®	SCC-002-009	FDA UDI	Class II	Active
Verteview®	VSA-200-044	FDA UDI	Class II	Active
Rebar®	SCC-001-005	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-02-8530	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-04-0007	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-03-0014	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
Jul 26, 2013	Z-1616-2016	—	terminated	The device was not appropriately set to mitigate the risk of implant fracture upon rotation inside the disc space.
Jun 4, 2009	Z-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.