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 26 of 60

Device	Model / Reference	Registries	Class	Status
2.7 VA Locking Screw	TRXV2.7-26 T	FDA UDI	Class II	Active
Sleds	MMSLED-35	FDA UDI	Class II	Active
Foot Plates	MMTP10L-6	FDA UDI	Class II	Active
Tools - WFS	BRG-SCREW	FDA UDI	Class I	Active
Cancellous Screw 3.8mm	CAB3.8-32	FDA UDI	Class II	Active
Tools - CFF	CFF-PLATE	FDA UDI	Class I	Active
Volar Fixed Angle Plates	VPPL-5-8	FDA UDI	Class II	Active
2.7 Locking Screw	TRXL2.7-48 T	FDA UDI	Class II	Active
Sleds	OSN-50	FDA UDI	Class II	Active
Torx Smooth Peg 2.3mm	SPEG2.3-42	FDA UDI	Class II	Active
Generic Instruments	GAUGWIR-1.6/100	FDA UDI	Class I	Active
Clavicle Plates	CPSMIDR-8	FDA UDI	Class II	Active
2.7 VA Locking Screw	TRXV2.7-42 T	FDA UDI	Class II	Unknown
Foot Plates	MCFR-17	FDA UDI	Class II	Active
Generic Instruments	BND-ASST	FDA UDI	Class I	Active
Hand Plates	PHT-12W	FDA UDI	Class II	Active
Foot Plates	LFR-8M	FDA UDI	Class II	Active
Foot Plates	LAPL-6	FDA UDI	Class II	Active
CannCompScrew 3.0mm (sst)	L3032 S	FDA UDI	Class II	Active
CLASSIC Dorsal/Ulnar Pin Plates	UPP7	FDA UDI	Class II	Active
HeadCannCompScrew 5.5mm	HS5552	FDA UDI	Class II	Active
Crosslock Screw	XLS3.4-48	FDA UDI	Class II	Active
Hex Cortical Screw 2.7mm	HEX2.7-50	FDA UDI	Class II	Active
HeadCannCompScrew 3.5mm	HL3535	FDA UDI	Class II	Active
Cancellous Screws 6.5mm	CAB6.5-28	FDA UDI	Class II	Active
CannCompScrew 1.7mm (Classic)	C1712	FDA UDI	Class II	Active
3.5 VA Locking Screw	HEXV3.5-38 T	FDA UDI	Class II	Active
Volar Shear Plates	VSP-R	FDA UDI	Class II	Active
2.7 Locking Screw	TRXL2.7-38 T	FDA UDI	Class II	Active
Locking HEX Screw 3.2mm	LHEX3.2-35	FDA UDI	Class II	Active
Tools - WFS (C)	WFS-LWR	FDA UDI	Class I	Active
Foot Plates	MFW2-2	FDA UDI	Class II	Active
HeadCannCompScrew 1.7mm	HL1707	FDA UDI	Class II	Active
Torx Smooth Peg 2.3mm	SPEG2.3-36	FDA UDI	Class II	Active
3.5 VA Locking Screw	HEXV3.5-26 T	FDA UDI	Class II	Active
HeadCannCompScrew 5.5mm	HS5544	FDA UDI	Class II	Active
Tools - HPS	PLRBNDR	FDA UDI	Class I	Active
Foot Plates	TN-7	FDA UDI	Class II	Active
Washers	WASHR-2.4	FDA UDI	Class II	Active
FPS Non-Locking Screw 2.7mm	CNS2.7-36	FDA UDI	Class II	Active
CannCompScrew 4.5mm (SelfDrill)	S4560	FDA UDI	Class II	Active
Hex Cortical Screw 3.2mm	HEX3.2-10	FDA UDI	Class II	Active
Volar Bearing Plates	VBEAR-3-7S	FDA UDI	Class II	Active
SmallThreadedIMNail 2.1mm (Ti)	IMN2.1-55 T	FDA UDI	Class II	Active
Generic Instruments	PLTBNDR-CFS	FDA UDI	Class I	Active
FMS Screw 5.5mm	JHEX5540	FDA UDI	Class II	Active
CannCompScrew 5.5mm (SelfDrill)	S5542	FDA UDI	Class II	Active
Fusion Cups	STF-CUP-S	FDA UDI	Class II	Active
CannCompScrew 4.5mm (SelfDrill)	S4564	FDA UDI	Class II	Active
Tools - TSS	DISTRS-TSS	FDA UDI	Class I	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.