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Trilliant Surgical LLC

Last updated September 17, 2026

Information

Country: US
Address: 727 N. Shepherd Dr, Houston, TX, 77007
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3007420745
DUNS Number: —

Catalogue (1635)

Page 24 of 33

Device	Model / Reference	Registries	Class	Status
Tiger	203-20-038	FDA UDI	Class II	Active
Tiger	200-45-160	FDA UDI	Class II	Active
Tiger	201-24-140	FDA UDI	Class II	Active
4.0mm x 40mm Gridlock Locking Screw	302-40-040	FDA UDI	Class II	Active
Arsenal Foot	330-01-206	FDA UDI	Class I	Active
Ankle Plate Module Insert	320-01-999	FDA UDI	Class I	Active
3S Hemi	111-00-001	FDA UDI	Class I	Active
Arsenal Ankle	309-45-105	FDA UDI	Class II	Active
Arsenal Ankle	309-45-100	FDA UDI	Class II	Active
Arsenal Foot	330-00-008	FDA UDI	Class I	Active
Arsenal Ankle	300-92-002	FDA UDI	Class II	Active
Arsenal Foot	307-40-012	FDA UDI	Class II	Active
Arsenal Foot	300-88-001	FDA UDI	Class II	Active
2.4mm/3.0mm Gridlock Screw Countersink	310-30-002	FDA UDI	Class I	Active
Tiger	201-40-230	FDA UDI	Class II	Active
8mm x 8mm x 8mm Staple	500-08-101	FDA UDI	Class II	Active
Tiger	203-30-026	FDA UDI	Class II	Active
Tiger	210-00-008	FDA UDI	Class I	Active
20mm x 20mm x 20mm High Strength Staple	500-20-201	FDA UDI	Class II	Active
4.0mm x 36mm Gridlock Locking Screw	302-40-036	FDA UDI	Class II	Active
3S Hemi	111-00-007	FDA UDI	Class I	Active
Arsenal Ankle	300-97-001	FDA UDI	Class II	Active
Arsenal Foot	308-40-026	FDA UDI	Class II	Active
Arsenal Ankle	309-45-065	FDA UDI	Class II	Active
Tiger	203-30-020	FDA UDI	Class II	Active
Tiger	203-40-242	FDA UDI	Class II	Active
Tiger	203-20-042	FDA UDI	Class II	Active
Tiger	202-45-024	FDA UDI	Class II	Active
Tiger	207-70-105	FDA UDI	Class II	Active
Tiger	200-24-040	FDA UDI	Class II	Active
Tiger	210-60-006	FDA UDI	Class I	Active
4.0mm x 38mm Gridlock Screw	301-40-038	FDA UDI	Class II	Active
Arsenal Ankle	300-90-002	FDA UDI	Class II	Active
Tiger	201-20-036	FDA UDI	Class II	Active
Arsenal Ankle	300-91-002	FDA UDI	Class II	Active
Arsenal Foot	300-80-006	FDA UDI	Class II	Active
Two-Step Hammertoe	204-30-114	FDA UDI	Class II	Active
Tiger	200-40-036	FDA UDI	Class II	Active
Tiger	205-70-085	FDA UDI	Class II	Active
3S Hemi	111-00-004	FDA UDI	Class I	Active
Arsenal Ankle	300-95-001	FDA UDI	Class II	Active
Arsenal Foot	308-40-028	FDA UDI	Class II	Active
2.4mm x 16mm Gridlock Locking Screw	302-24-016	FDA UDI	Class II	Active
7mm Disco Subtalar Trial	112-20-007	FDA UDI	Class I	Active
Tiger	210-00-001	FDA UDI	Class I	Active
STAR PSI Tibia Anatomical Model	601-01-001	FDA UDI	Class III	Active
Tiger	211-01-212	FDA UDI	Class I	Active
Tiger	210-99-103	FDA UDI	Class I	Active
Tiger	203-30-044	FDA UDI	Class II	Active
Arsenal Foot	300-81-007	FDA UDI	Class II	Active

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FDA Recalls (24)

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
Nov 4, 2019	Z-1635-2020	—	terminated	The firm has identified that parts from the kit, lot: TSL007202, have the potential to contain the incorrect contents of the 8mm HTR Sterile Hammer Toe Reaming Kit. The kit should contain (2) reamers total, (1) Concave Reamer and (1) Convex Reamer; there is the potential that kits from the identified lot may have (2) of the same reamer type as opposed to one (1) of each type.
Oct 10, 2019	Z-1892-2020	—	terminated	Labeling Error; specifically, drill bits from lots # TSL008495A are marked with the lot # of TSL008495. This could lead to parts being misidentified and impact device traceability.
Mar 14, 2019	Z-0799-2020	—	terminated	A screwdriver used to facilitate implant insertion and removal was found to be out of specification for the minor diameter of the drive feature causing the driver to be unable to retain screws as intended.
Jul 19, 2018	Z-1608-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1612-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1614-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1610-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1609-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1605-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1611-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1606-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1607-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Jul 19, 2018	Z-1613-2020	—	terminated	Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Mar 27, 2018	Z-2339-2018	—	terminated	Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation of function with the adapter collar sticking, and/or not retaining the mating adapter male shaft.
Mar 27, 2018	Z-2338-2018	—	terminated	Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation of function with the adapter collar sticking, and/or not retaining the mating adapter male shaft.
Dec 8, 2016	Z-0960-2017	—	terminated	Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to the field with a printing error where k-wire description markings indicate diameters of 0.45 and 0.35 instead of 0.045" and 0.035", respectively.
Sep 2, 2016	Z-0609-2017	—	terminated	Screws were identified as having the incorrect part number and lot number marked upon them. The part number incorrectly indicated a length of 115 mm rather than 110 mm. The lot number incorrectly indicated lot number of TSL003765 rather than TSL003721.
Aug 6, 2015	Z-2490-2015	—	terminated	The affected parts subject to the recall are out of specification, resulting in in the loss of the optimal locking screw functionality of the plates. The thread depth of the screw holes is insufficient, potentially limiting the ability to engage and lock with associated mating locking screws.
Jul 31, 2015	Z-2738-2015	—	terminated	Gridlock screw driver bits for the Gridlock Plating System were identified to be out of specification and have the potential for shallow engagement between the driver and the screw, resulting in an increased likelihood of stripping screw heads intraoperatively. Specifically, the minor diameter of the drive feature is above the specification, potentially reducing the engagement between the driver and the screw head.
Jul 20, 2015	Z-2452-2015	—	terminated	The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too small to allow for the guide wire to pass completely through.
Jul 20, 2015	Z-2421-2015	—	terminated	The cutting efficiency of the Countersinks was out of specification.
Jul 20, 2015	Z-2456-2015	—	terminated	The cannulation of the Concave and Convex Reamer Heads may be too small to allow the Guide Pin to freely pass through.
Jul 20, 2015	Z-2464-2015	—	terminated	Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw Systems were reported to occasionally be difficult to remove from the sterilization tray.
Apr 14, 2009	Z-1438-2010	—	terminated	Firm received several complaints of field failures, e.g., "broke during surgery" and the firm initiated a design change. A communication to sales staff 04/14/2009 instructed them to recover and reconcile these products from user physicians.