Is this your brand? Sign in to claim ownership.

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 5 of 19

Device	Model / Reference	Registries	Class	Status
Apelo® / Apelo® MIS	1110-01-7540	FDA UDI	Class II	Active
V3” Segmental Plating System	1121-05-0020	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-05-6066	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-7560	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-08-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-11-0000	FDA UDI	Class I	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-40-0000	FDA UDI	Class I	Active
HiJAK™ Stand Alone	1123-01-0013	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-7550	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-7560	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-09-0013	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-6545	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-08-0090	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	5006-03-0000	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-13-0450	FDA UDI	Class I	Active
Verteview®	VSA-400-086	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-02-0014	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-4545	FDA UDI	Class II	Active
Rebar®	SCC-001-011	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-04-0007	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-6550	FDA UDI	Class II	Active
V3” Segmental Plating System	1121-05-0009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-13-0850	FDA UDI	Class I	Active
Verteview®	VSA-100-034	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-03-8530	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-10-0085	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-6545	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-14-0400	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-02-4525	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-47-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-40-0000	FDA UDI	Class I	Active
Verteview®	VSA-100-022	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-68-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-58-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1100-08-0065	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-14-0085	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-06-0000	FDA UDI	Class I	Active
V3” Segmental Plating System	1121-05-0017	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-41-0000	FDA UDI	Class I	Active
HiJAK™ Cervical	1119-08-0009	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-08-0010	FDA UDI	Class II	Active
Verteview®	VSA-400-089	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-14-0500	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-16-0040	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

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.

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.