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 11 of 19

Device	Model / Reference	Registries	Class	Status
HiJAK™ Stand Alone	1123-03-0013	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-09-0010	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-04-0008	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1106-01-4535	FDA UDI	Class II	Active
HiJAK™ Stand Alone	1123-02-0011	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-02-7555	FDA UDI	Class II	Active
Verteview®	VSS-042-016	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	7006-02-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2010-81-0550	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-18-0000	FDA UDI	Class I	Active
Verteview®	VSA-300-054	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Verteview®	VSS-046-012	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0002	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-01-5545	FDA UDI	Class II	Active
Verteview®	VSA-200-046	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-02-0008	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-01-0018	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-09-0007	FDA UDI	Class II	Active
Stature®	STL-015-012	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-07-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2009-01-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1100-10-0040	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-6530	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-02-6530	FDA UDI	Class II	Active
HiJAK™ Cervical	1119-05-0007	FDA UDI	Class II	Active
True Position®	True Position®	FDA UDI	Class II	Active
Verteview®	VSS-042-212	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-03-8545	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-73-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1100-10-0060	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1110-02-6560	FDA UDI	Class II	Active
HiJAK™ Stand Alone	1123-01-0014	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-10-0030	FDA UDI	Class II	Active
HiJAK™ Cervical	2019-07-0014	FDA UDI	Class II	Active
V3™ Segmental Plating System	1121-04-0014	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	5010-02-0000	FDA UDI	Class I	Active
HiJAK™ Cervical	2019-05-0009	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	6910-23-0750	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1100-05-0020	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	1110-01-7545	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-76-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	1100-08-0045	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2010-05-0000	FDA UDI	Class I	Active
Apelo® / Apelo® MIS	2006-13-0525	FDA UDI	Class I	Active
HiJAK™ Cervical	1119-01-0012	FDA UDI	Class II	Active
Apelo® / Apelo® MIS	2006-34-0000	FDA UDI	Class I	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.