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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 13 of 19

Device	Model / Reference	Registries	Class	Status
Apelo® / Apelo® MIS	1100-01-0100	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-04-0009	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-09-0007	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Verteview®	VSA-100-028	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0008	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6006-08-0000	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-10-0012	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-04-0013	FDA UDI	Class II	Active
Rebar®	SCC-002-011	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-25-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1100-14-0070	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-60-0000	FDA UDI	Class I	Active
HiJAK™ Cervical	2019-03-0008	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-74-0000	FDA UDI	Class I	Active
V3™ Segmental Plating System	1121-02-0016	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-03-0100	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-13-0625	FDA UDI	Class I	Active
HiJAK™ Cervical	1119-10-0008	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-8530	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-01-8550	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-8540	FDA UDI	Class II	Active
Verteview®	VSA-300-066	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-73-0000	FDA UDI	Class I	Active
HiJAK™ Cervical	1119-09-0013	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-10-0060	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-04-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-70-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1110-02-4535	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-07-0000	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0085	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-52-0000	FDA UDI	Class I	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6910-19-0000	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-10-0045	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-8540	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2000-01-0000	FDA UDI	Class I	Active
HiJAK™ Cervical	1119-09-0011	FDA UDI	Class II	Active
V3™ Segmental Plating System	1121-02-0014	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-01-0007	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-6560	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0015	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-05-4248	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-4535	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-7550	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-04-0012	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-05-0011	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.