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OSSEUS FUSION SYSTEMS LLC

Last updated September 17, 2026

Information

Country: US
Address: 1931 Greenville Avenue, Dallas, TX, 75206
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3010531060
DUNS Number: —

Catalogue (1382)

Page 28 of 28

Device	Model / Reference	Registries	Class	Status
Aries-L Lateral Lumbar Interbody System	1400-0241	FDA UDI	Class II	Active
Aries-TS TSLIF Lumbar Interbody System	1100-0522S	FDA UDI	Class II	Active
Aries-TS TSLIF Lumbar Interbody System	1100-0128S	FDA UDI	Class II	Active
White Pearl Preferred Angle ACP	2100-6016	FDA UDI	Class II	Active
Aries-L Lateral Lumbar Interbody System	1450-8110	FDA UDI	Class I	Active
Aries-TS TSLIF Lumbar Interbody System	1100-0524S	FDA UDI	Class II	Active
Aries-L Lateral Lumbar Interbody System	1450-8210	FDA UDI	Class I	Active
Aries-TS TSLIF Lumbar Interbody System	1100-1521S	FDA UDI	Class II	Active
White Pearl Preferred Angle ACP	2100-9718	FDA UDI	Class II	Active
White Pearl Preferred Angle ACP	2100-0514	FDA UDI	Class II	Active
Aries-TC	1250-6010	FDA UDI	Class I	Active
White Pearl Preferred Angle ACP	2100-3142	FDA UDI	Class II	Active
Aries-TC	1200-1204	FDA UDI	Class II	Active
White Pearl Preferred Angle ACP	2100-0212	FDA UDI	Class II	Active
Aries-L Lateral Lumbar Interbody System	1450-1241	FDA UDI	Class I	Active
White Pearl Preferred Angle ACP	2100-0820	FDA UDI	Class II	Active
Aries-TC	1200-0706	FDA UDI	Class II	Active
Aries-TS TSLIF Lumbar Interbody System	1100-0523S	FDA UDI	Class II	Active
White Pearl Preferred Angle ACP	2100-0812	FDA UDI	Class II	Active
Aries-L Lateral Lumbar Interbody System	1450-8012	FDA UDI	Class I	Active
Aries-L Lateral Lumbar Interbody System	1400-5240	FDA UDI	Class II	Active
White Pearl Preferred Angle ACP	2100-9112	FDA UDI	Class II	Active
Osseus Black Diamond Pedicle Screw System	K131810	FDA 510(k)	Class II	Active
Pisces™-SA STANDALONE ALIF Interbody System	K223413	FDA 510(k)	Class II	Active
PISCES-SA Standalone ALIF Interbody System	K213935	FDA 510(k)	Class II	Active
Black Diamond Navigation Instruments	K192495	FDA 510(k)	Class II	Active
Aries® Lumbar Interbodies	K181347	FDA 510(k)	Class II	Active
Black Diamond™ POCT Spinal System	K222107	FDA 510(k)	Class II	Active
Blue Topaz Sacroiliac Screw System	K213590	FDA 510(k)	Class II	Active
Black Diamond Pedicle Screw System	K192121	FDA 510(k)	Class II	Active
White Pearl Preferred Angle Anterior Cervical Plate	K160522	FDA 510(k)	Class II	Active
Gemini-C Hybrid Cervical Interbody System	K170844	FDA 510(k)	Class II	Active

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