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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 2 of 19

Device	Model / Reference	Registries	Class	Status
Apelo® / Apelo® MIS	1100-05-0032	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0075	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-14-0300	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-05-0030	FDA UDI	Class II	Active
Stature®	STF-013-010	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0040	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-10-0080	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6910-20-0450	FDA UDI	Class II	Active
Verteview®	VSS-042-114	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-11-0000	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-16-0200	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-7560	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
V3™ Segmental Plating System	1121-02-0012	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-08-0008	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-8540	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6006-09-0000	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-09-0008	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2012-78-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1110-01-8545	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-03-0008	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-16-0100	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-04-0000	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-08-0013	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-7530	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-10-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-05-5460	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-8535	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-07-0009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-80-0000	FDA UDI	Class I	Active
True Position®	True Position®	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-08-0012	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-16-0035	FDA UDI	Class II	Active
HiJAK™ Stand Alone	1123-03-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-01-0030	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-8550	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
V3™ Segmental Plating System	1121-04-0016	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6906-33-0550	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-7545	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-72-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1100-16-0110	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0007	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-01-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-16-0000	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

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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.