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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 7 of 33

Device	Model / Reference	Registries	Class	Status
Tiger	203-20-022	FDA UDI	Class II	Active
Tiger	203-24-014	FDA UDI	Class II	Active
Tiger	215-00-004	FDA UDI	Class I	Active
Tiger	203-40-250	FDA UDI	Class II	Active
3.5mm x 20mm Gridlock Ankle Screw	304-35-020	FDA UDI	Class II	Active
Tiger	203-20-032	FDA UDI	Class II	Active
Tiger	201-24-030	FDA UDI	Class II	Active
Tiger	205-70-001	FDA UDI	Class II	Active
Tiger	211-40-002	FDA UDI	Class I	Active
9 Hole 1/3 Tubular Gridlock Ankle Plate	300-63-002	FDA UDI	Class II	Active
Tiger	215-55-003	FDA UDI	Class I	Active
4.0mm x 60mm Gridlock Ankle Syndesmotic Screw LP	306-41-060	FDA UDI	Class II	Active
10mm Convex Reamer	220-10-002	FDA UDI	Class I	Active
4 Hole VL Gridlock Plate	300-55-003	FDA UDI	Class II	Active
Tiger	203-40-224	FDA UDI	Class II	Active
Tiger	201-30-146	FDA UDI	Class II	Active
Tiger	200-40-048	FDA UDI	Class II	Active
Tiger	201-40-050	FDA UDI	Class II	Active
11mm Disco Subtalar Implant	102-20-011	FDA UDI	Class II	Active
Arsenal Foot	300-82-025	FDA UDI	Class II	Active
Minimally Invasive Bunion Plate, Right	300-70-001	FDA UDI	Class II	Active
3S Hemi	111-00-010	FDA UDI	Class I	Active
Tiger	200-45-001	FDA UDI	Class II	Active
Arsenal Foot	308-35-012	FDA UDI	Class II	Active
Arsenal Foot	308-40-048	FDA UDI	Class II	Active
Tiger	200-40-046	FDA UDI	Class II	Active
Arsenal Ankle	340-01-202	FDA UDI	Class I	Active
Tiger	201-40-256	FDA UDI	Class II	Active
Tiger	211-01-201	FDA UDI	Class I	Active
Tiger	202-20-024	FDA UDI	Class II	Active
Tiger	340-15-007	FDA UDI	Class I	Active
3.0mm x 28mm Gridlock Screw	301-30-028	FDA UDI	Class II	Active
Arsenal Foot	307-22-012	FDA UDI	Class II	Active
Arsenal Foot	308-27-014	FDA UDI	Class II	Active
3.0mm x 14mm Gridlock Locking Screw	302-30-014	FDA UDI	Class II	Active
Tiger	210-00-101	FDA UDI	Class I	Active
Arsenal Foot	300-81-002	FDA UDI	Class II	Active
Tiger	203-40-214	FDA UDI	Class II	Active
Tiger	203-20-018	FDA UDI	Class II	Active
Tiger	202-30-014	FDA UDI	Class II	Active
2.7mm x 12mm Gridlock Ankle Locking Screw	305-27-012	FDA UDI	Class II	Active
Tiger	213-30-002	FDA UDI	Class I	Active
Tiger	200-30-026	FDA UDI	Class II	Active
Tiger	206-70-050	FDA UDI	Class II	Active
Tiger	200-20-022	FDA UDI	Class II	Active
Arsenal Ankle	309-45-110	FDA UDI	Class II	Active
Arsenal Foot	311-02-020	FDA UDI	Class I	Active
Subtalar Implant System Sterilization Tray Lid	112-99-011	FDA UDI	Class I	Active
4.0mm x 24mm Cannulated Screw	201-40-024	FDA UDI	Class II	Active
Tiger	200-45-003	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.