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Titan Spine, Inc.

Last updated May 23, 2026

Information

Country: US
Address: —
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FDA FEI Number: —
DUNS Number: —

Catalogue (5505)

Page 1 of 111

Device	Model / Reference	Registries	Class	Status
Endoskeleton Tcs	5086-1605	FDA UDI	Class II	Unknown
Endoskeleton TL	7100-2315-N	FDA UDI	Class II	Unknown
Endoskeleton® Tl	7112-2213	FDA UDI	Class II	Unknown
Endoskeleton TC	5180-1608	FDA UDI	Class II	Unknown
Endoskeleton TL	7107-2514-S	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology	7120-0515-N	FDA UDI	Class II	Unknown
Endoskeleton TL	7100-1116-N	FDA UDI	Class II	Unknown
Endoskeleton TAS	2312-0315-N	FDA UDI	Class II	Unknown
Endoskeleton Tt	4200-1050	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology	7124-0319-N	FDA UDI	Class II	Unknown
ENDOSKELETON® TAS Sterile Barrier System	2312-0212-S	FDA UDI	Class II	Unknown
Endoskeleton TL	7100-0109-S	FDA UDI	Class II	Unknown
Endoskeleton TL	7100-1115	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology	7120-2116-N	FDA UDI	Class II	Unknown
Endoskeleton® Tl	7107-2416	FDA UDI	Class II	Unknown
Endoskeleton® Tl	7100-2108	FDA UDI	Class II	Unknown
ENDOSKELETON® TL nanoLOCK® Surface Technology	7107-2308-N	FDA UDI	Class II	Unknown
Endoskeleton TL	7107-1514	FDA UDI	Class II	Unknown
Endoskeleton® Tl	7200-1134	FDA UDI	Class II	Unknown
Endoskeleton TO	3114-2211-N	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology	7116-1414-N	FDA UDI	Class II	Unknown
Endoskeleton TL	7112-1309-S	FDA UDI	Class II	Unknown
Endoskeleton TL	7112-2415-S	FDA UDI	Class II	Unknown
Endoskeleton® Tcs	5301-3815	FDA UDI	Class II	Unknown
Endoskeleton TL	7112-1309	FDA UDI	Class II	Unknown
Endoskeleton TCS	5301-3516	FDA UDI	Class II	Unknown
Endoskeleton® Ta	2112-9320	FDA UDI	Class II	Unknown
Endoskeleton TL	7107-2513	FDA UDI	Class II	Unknown
Endoskeleton Tcs	5066-1411	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Hyperlordotic	7220-0520	FDA UDI	Class II	Unknown
Endoskeleton® Tt	4214-2513	FDA UDI	Class II	Active
ENDOSKELETON® TL nanoLOCK® Surface Technology	7112-2515-N	FDA UDI	Class II	Unknown
Endoskeleton TO	3110-3110	FDA UDI	Class II	Unknown
Endoskeleton® Tc	5180-1607	FDA UDI	Class II	Unknown
Endoskeleton TCS	5360-1411-S	FDA UDI	Class II	Unknown
ENDOSKELETON® TL nanoLOCK® Surface Technology	7107-2508-N	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology	7130-2220-N	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Sterile Barrier System	7112-0215-S	FDA UDI	Class II	Unknown
Endoskeleton® Tl	7107-2209	FDA UDI	Class II	Unknown
Endoskeleton® Dpk	831-1005-0	FDA UDI	Class I	Unknown
ENDOSKELETON Posterior DPK	1100-0017	FDA UDI	Class I	Unknown
Endoskeleton® To	3900-1011	FDA UDI	Class II	Unknown
Endoskeleton® To	3210-0001	FDA UDI	Class II	Unknown
Endoskeleton® Tl	7200-1080	FDA UDI	Class II	Unknown
ENDOSKELETON® TAS Hyperlordotic Sterile Barrier System	2316-0114-S	FDA UDI	Class II	Unknown
ENDOSKELETON® TT Sterile Barrier System	4114-2514-S	FDA UDI	Class II	Unknown
ENDOSKELETON® TL Sterile Barrier System	7112-2309-S	FDA UDI	Class II	Unknown
Endoskeleton TL	7107-2216	FDA UDI	Class II	Unknown
Endoskeleton® Tl	7212-1509	FDA UDI	Class II	Unknown
ENDOSKELETON® TL nanoLOCK® Surface Technology	7100-1309-N	FDA UDI	Class II	Unknown

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FDA Recalls (3)

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 20, 2015	Z-2327-2015	—	terminated	Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.
Feb 20, 2015	Z-1324-2015	—	terminated	The TCS Straight Hexlobular #6 Drivers (5210-1004) tip sheared off during use in procedures that involved patients with dense bones. As a result of this malfunction, Titan Spine, LLC is removing all of the TCS Straight Hex lobular #6 Drivers (5210-1004) Lot# G150101 from the field.
Oct 19, 2012	Z-0535-2013	—	terminated	Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products. The labeling accompanying this device contains incorrect indications for use.