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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 44 of 60

Device	Model / Reference	Registries	Class	Status
Tools - TWF	RFP-TRAY	FDA UDI	Class I	Active
Cancellous Screw 3.8mm	CAB3.8-12	FDA UDI	Class II	Active
CannCompScrew 3.0mm (SelfDrill)	L3021	FDA UDI	Class II	Active
CannCompScrew 3.5mm (Classic)	C3518	FDA UDI	Class II	Active
Hex Cortical Screw 4.0mm	HEX4.0-50	FDA UDI	Class II	Active
CannCompScrew 4.5mm (Classic)	C4564	FDA UDI	Class II	Active
Tools - CFF	CFF-SCREW-LID	FDA UDI	Class I	Active
Tools - HPS	DVCX-3.0/070 J	FDA UDI	Class I	Active
3.5 VA Locking Screw	TRXV3.5-30 T	FDA UDI	Class II	Active
Tools - Screws	DVHX-2.5/130C AO	FDA UDI	Class I	Active
Calcaneal Plates	CLSR-09	FDA UDI	Class II	Active
Foot Plates	MTPL-7	FDA UDI	Class II	Active
Tools-Screws	DVHX-2.4/070MC AO	FDA UDI	Class I	Active
Generic Instruments	THNDL	FDA UDI	Class I	Active
CannCompScrew 3.0mm (SelfDrill)	S3018	FDA UDI	Class II	Active
FPS Non-Locking Screw 3.5mm	CNS3.5-30	FDA UDI	Class II	Active
Torx Cortical Screw	TRX2.3-21	FDA UDI	Class II	Active
Tools - AFS	MPP-GUIDE	FDA UDI	Class I	Active
CannCompScrew 7.3mm (Classic)	C7352	FDA UDI	Class II	Active
HeadCannCompScrew 3.0mm	HL3037	FDA UDI	Class II	Active
Tools - FPS	GUIDE-L2.3	FDA UDI	Class I	Active
Foot Plates	MTPL-7S	FDA UDI	Class II	Active
4.0 Cortical Screw	TRXC4.0-12 T	FDA UDI	Class II	Active
Locking Cortical Screw 2.7mm	LCBS2.7-16	FDA UDI	Class II	Active
CannCompScrew 3.5mm (SelfDrill)	L3510	FDA UDI	Class II	Active
Tools - HCS	CANNULA-3.5	FDA UDI	Class I	Active
HeadCannCompScrew 7.3mm	HL7392	FDA UDI	Class II	Active
CannCompScrew 5.5mm (SelfDrill)	L5548	FDA UDI	Class II	Active
Tools - HPS	HPS-PLT/SCRW1.5	FDA UDI	Class I	Active
CLASSIC Dorsal/Ulnar Pin Plates	UPP3	FDA UDI	Class II	Active
2.3 Locking Screw	TRXL2.3-12 T	FDA UDI	Class II	Active
Tools - DHF	SLVWIRE-2.0/125	FDA UDI	Class I	Active
HPS Cortical Screw 2.0mm	MCCS2.0-10	FDA UDI	Class II	Active
Tools - Screws	TXDRIVR-8/180 AO	FDA UDI	Class I	Active
HeadCannCompScrew 2.3mm	HL2312	FDA UDI	Class II	Active
Hcs-Screwlid1.7	HCS-SCREWLID1.7	FDA UDI	Class I	Active
Tools - INS	INS-CADDY2.4/2.7-LID	FDA UDI	Class I	Active
Volar Fixed Angle Plates	VPPR-3-7N	FDA UDI	Class II	Active
Tools - WS3	GDWHKD-1.8	FDA UDI	Class I	Active
Cancellous Screws 6.5mm	CAB6.5-40	FDA UDI	Class II	Active
4.0 VA Locking Screw	TRXV4.0-32 T	FDA UDI	Class II	Active
2.7 Cortical Screw	HEXC2.7-14 T	FDA UDI	Class II	Active
Foot Plates	MCFL-17	FDA UDI	Class II	Active
Tools - WS3	SBOLT2.4-22	FDA UDI	Class I	Active
Tools - WFS	GUIDEPEG-1.8 NW	FDA UDI	Class I	Active
Cortical Screws 2.3mm	CBS2.3-32	FDA UDI	Class II	Active
Foot Plates	SP20-6	FDA UDI	Class II	Active
3.5 Cortical Screw	TRXC3.5-30 T	FDA UDI	Class II	Active
Tools - UOS	UOSG-A-2	FDA UDI	Class I	Active
S.A. - Volar Bearing Plates	VLBPL-5-5 (C)	FDA UDI	Class II	Active

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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.