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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 1 of 19

Device	Model / Reference	Registries	Class	Status
HiJAK™ Cervical	1119-03-0009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6900-06-0450	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-17-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1106-01-8530	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0013	FDA UDI	Class II	Active
Verteview®	VSS-042-112	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0070	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Stature®	STF-011-008	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-63-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-62-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-35-0000	FDA UDI	Class I	Active
Rebar®	SCC-002-010	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-66-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-31-0000	FDA UDI	Class I	Active
HiJAK™ Cervical	1119-08-0014	FDA UDI	Class II	Active
HiJAK™ Stand Alone	1123-02-0010	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-81-0350	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-61-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1110-02-7530	FDA UDI	Class II	Active
HiJAK™ Stand Alone	1123-04-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-16-0400	FDA UDI	Class II	Active
V3™ Segmental Plating System	1121-01-0009	FDA UDI	Class II	Active
HiJAK™ Stand Alone	1123-03-0012	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-01-6540	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-05-0008	FDA UDI	Class II	Active
Verteview®	VSA-300-057	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-6530	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-6540	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2009-67-0000	FDA UDI	Class I	Active
True Position®	True Position®	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-08-0011	FDA UDI	Class II	Active
HiJAK™ Stand Alone	1123-04-0013	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-03-0009	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0000	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-8560	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-02-0013	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0010	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-03-0050	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0110	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0050	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-02-7560	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-14-0090	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-55-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-28-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1100-01-0095	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-09-0004	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-59-0000	FDA UDI	Class I	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.