Is this your brand? Sign in to claim ownership.

Trimed, INC.

Last updated September 17, 2026

Information

Country: US
Address: 27533 Avenue Hopkins, Santa Clarita, CA, 91355
Website: trimedortho.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(661)255-7406
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3001236812
DUNS Number: 138041277

Catalogue (2974)

Page 13 of 60

Device	Model / Reference	Registries	Class	Status
Cancellous Screw 3.8mm	CAB3.8-20	FDA UDI	Class II	Active
Foot Plates	LAP8R-5	FDA UDI	Class II	Active
Foot Plates	MFU-14	FDA UDI	Class II	Active
3.5 Cortical Screw	TRXC3.5-40 T	FDA UDI	Class II	Active
Tools - HCS	CSINK-3.0	FDA UDI	Class I	Active
CannCompScrew 3.5mm (SelfDrill)	L3544	FDA UDI	Class II	Active
Tools - Screws	GRIPRHX-2.5	FDA UDI	Class I	Active
Tools - TSS	TSS-TRAY	FDA UDI	Class I	Active
Tools - HCS	CSS-SCREW2.3	FDA UDI	Class I	Active
Clavicle Plates	CPSLATL-15	FDA UDI	Class II	Active
Foot Plates	LP35-3	FDA UDI	Class II	Active
CannCompScrew 3.5mm (SelfDrill)	L3529	FDA UDI	Class II	Active
Hand Plates	PHS-6	FDA UDI	Class II	Active
Foot Plates	MCFL-9	FDA UDI	Class II	Active
SmallThreadedIMNail 2.1mm (Ti)	IMN2.1-25 T	FDA UDI	Class II	Active
Volar Fixed Angle Plates	VFPL-7-7S	FDA UDI	Class II	Active
2.3 VA Locking Screw	TRXV2.3-28 T	FDA UDI	Class II	Active
Tools - FPS	XPANDRT15	FDA UDI	Class I	Active
HeadCannCompScrew 1.7mm	HL1706	FDA UDI	Class II	Active
2.3 Cortical Screw	TRXC2.3-22 T	FDA UDI	Class II	Active
SmallThreadedIMNail 3.0mm (sst)	IMN3.0-65 S	FDA UDI	Class II	Active
Tools - INS	INS-CADDY-3.0/3.6	FDA UDI	Class I	Active
Torx Threaded Peg	TPEG-14	FDA UDI	Class II	Active
Washers	WASHR	FDA UDI	Class II	Active
2.7 Cortical Screw	HEXC2.7-50 T	FDA UDI	Class II	Active
Hex Cortical Screw 3.2mm	HEX3.2-15	FDA UDI	Class II	Active
SmallThreadedIMNail 2.1mm (sst)	IMN2.1-55 S	FDA UDI	Class II	Active
Hex Cortical Screw 3.2mm	HEX3.2-39	FDA UDI	Class II	Active
3.5 VA Locking Screw	TRXV3.5-48 T	FDA UDI	Class II	Active
CannCompScrew 7.3mm (Classic)	CL7384	FDA UDI	Class II	Active
CannCompScrew 7.3mm (SelfDrill)	L7380	FDA UDI	Class II	Active
Foot Plates	MTP10L-6	FDA UDI	Class II	Active
Locking Cortical Screw 3.2mm	LCBS3.2-18	FDA UDI	Class II	Active
Tools-SHD	HDSINK-2.3	FDA UDI	Class I	Active
Tools - Screws	DVHX-3.5/130C AO	FDA UDI	Class I	Active
Tools - FPS	BNDROD-S	FDA UDI	Class I	Active
Tools - CFS	SHIELD	FDA UDI	Class I	Active
4.0 Cortical Screw	TRXC4.0-44 T	FDA UDI	Class II	Active
Calcaneal Plates	CLSR-08	FDA UDI	Class II	Active
Tools-Screws	DVTX-8/180 AO B	FDA UDI	Class I	Active
Drills	DRILL-2.30L	FDA UDI	Class I	Active
Tools - FPS	RMRFPSC-18	FDA UDI	Class I	Active
Tools - HCS	HSINK-3.0	FDA UDI	Class I	Active
Locking Cortical Screw 2.7mm	LCBS2.7-08	FDA UDI	Class II	Active
2.7 VA Locking Screw	HEXV2.7-22 T	FDA UDI	Class II	Active
FPS Locking Screw 3.5mm	CLS3.5-14	FDA UDI	Class II	Active
2.7 VA Locking Screw	TRXV2.7-40 T	FDA UDI	Class II	Active
Drills	DRILL-2.1CL	FDA UDI	Class I	Active
Tools - Screws	GAUGE-1.8	FDA UDI	Class I	Active
2.3 VA Locking Screw	TRXV2.3-20 T	FDA UDI	Class II	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 (18)

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
Mar 19, 2024	Z-1792-2024	—	open, classified	Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Mar 19, 2024	Z-1791-2024	—	open, classified	Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Nov 28, 2023	Z-0932-2024	—	open, classified	Plates, part of a wrist fixation system, are affixed during surgery with bearings that may pop out from distal peg holes.
Dec 22, 2022	Z-1101-2023	—	open, classified	Overly aggressive tension on the pull suture, while passing the medial button through a bone/soft tissue tunnel across the fibula and tibia, can exceed its strength causing it to break.
Sep 28, 2018	Z-0356-2020	—	open, classified	The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Sep 28, 2018	Z-0357-2020	—	open, classified	The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Sep 28, 2018	Z-0355-2020	—	open, classified	The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Sep 28, 2018	Z-0358-2020	—	open, classified	The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
Sep 28, 2018	Z-0359-2020	—	open, classified	The WHD/WHV impactors can rust over time due to an improper manufacturing process.
Aug 24, 2018	Z-1214-2019	—	terminated	The bone screw is shorter than the intended design specification.
Aug 24, 2018	Z-0118-2020	—	terminated	Modifications to the specification were not appropriately qualified through the company's design control process which may result in structural integrity issues of the device.
Aug 15, 2018	Z-0366-2020	—	terminated	The firm has become aware that the angled-hole of certain semi-tubular design bone plates may have been modified from its specification, and the modification may not have been fully qualified.
Apr 16, 2018	Z-2877-2018	—	terminated	Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate
Apr 13, 2018	Z-2265-2018	—	terminated	During a retrospective review of sterilization records, TriMed has determined that evidence of quarterly dose audits/verification required to comply with the regulations could not be found. Sterilization records indicate that all lots of staples were irradiated to at least the defined dose. There is a risk that this issue could result in patient infection if not properly sterilized.
Apr 13, 2018	Z-2264-2018	—	terminated	During a retrospective review of sterilization records, TriMed has determined that evidence of quarterly dose audits/verification required to comply with the regulations could not be found. Sterilization records indicate that all lots of staples were irradiated to at least the defined dose. There is a risk that this issue could result in patient infection if not properly sterilized.
Apr 13, 2018	Z-2263-2018	—	terminated	During a retrospective review of sterilization records, TriMed has determined that evidence of quarterly dose audits/verification required to comply with the regulations could not be found. Sterilization records indicate that all lots of staples were irradiated to at least the defined dose. There is a risk that this issue could result in patient infection if not properly sterilized.
Apr 13, 2018	Z-2262-2018	—	terminated	During a retrospective review of sterilization records, TriMed has determined that evidence of quarterly dose audits/verification required to comply with the regulations could not be found. Sterilization records indicate that all lots of staples were irradiated to at least the defined dose. There is a risk that this issue could result in patient infection if not properly sterilized.
Jan 11, 2018	Z-1373-2018	—	terminated	Following the completion of sterilization cycle(s) of the impacted Hex Driver, the epoxy color band on the impacted Hex Driver can migrate down the shaft and/or potentially onto the sterilization tray or caddy.