Data / Medical devices / United States / Symmetry Medical, Inc. - Manchester

Symmetry Medical, Inc. - Manchester: FDA-registered device maker in Manchester, NH, United States, 4 510(k) clearances

Name: Symmetry Medical, Inc. - Manchester FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Symmetry Medical, Inc. - Manchester is registered with the FDA (registration 1221053) in Manchester, NH, United States. It lists 41 device types. The FDA files 4 510(k) clearances under its listings, the newest dated October 22, 2004. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this one Watch Symmetry Medical, Inc. - Manchester

FDA registration number: 1221053
Address: 253 Abby Rd, Manchester, NH, United States, 03103
Owner or operator: Tecomet (1828464)
Roles: Contract manufacturer, Manufacturer
First device listed: August 5, 1992
Registered through: 2026
Brand names listed: 0 DEG CUT GUIDE, 10MM Dual Endoscopes Tray, 2.7mm Office Hysteroscope Tray, 3 DEG CUT GUIDE, 3.5 mm Implant Module, Assembly, Proximal Tibia Plate, 3.5 mm Implant Module, Base, Proximal Tibia Plate, 3x7 W/logo Blue Mat Xomed, R1063, 4.5 mm Implant Module, Assembly, Proximal Tibia Plate and more

Devices it lists

Device	Product code	Class	Role	Source
Appliance, Fixation, Spinal Interlaminal	KWP	2	Contract manufacturer	accessdata.fda.gov
Appliance, Fixation, Spinal Intervertebral Body	KWQ	2	Contract manufacturer	accessdata.fda.gov
Cerclage, Fixation	JDQ	2	Contract manufacturer	accessdata.fda.gov
Dental Implant Surgical Tray	OFY	1	Contract manufacturer	accessdata.fda.gov
Device, Fixation, Proximal Femoral, Implant	JDO	2	Contract manufacturer	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Contract manufacturer	accessdata.fda.gov
Guide, Surgical, Instrument	FZX	1	Contract manufacturer	accessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment	HWE	1	Contract manufacturer	accessdata.fda.gov
Instrument, Ultrasonic Surgical	LFL	U	Contract manufacturer	accessdata.fda.gov
Integrated Operating Table-Electromechanical Surgical System	SIR	2	Contract manufacturer	accessdata.fda.gov
Intervertebral Fusion Device With Bone Graft, Lumbar	MAX	2	Contract manufacturer	accessdata.fda.gov
Mesh, Surgical, Acetabular, Hip, Prosthesis	JDJ	2	Contract manufacturer	accessdata.fda.gov
Neurosurgical Ultrasonic Instruments	LBK	U	Contract manufacturer	accessdata.fda.gov
Orthopedic Stereotaxic Instrument	OLO	2	Contract manufacturer	accessdata.fda.gov
Orthopedic Tray	OJH	1	Contract manufacturer	accessdata.fda.gov
Orthosis, Spinal Pedicle Fixation	MNI	2	Contract manufacturer	accessdata.fda.gov
Orthosis, Spondylolisthesis Spinal Fixation	MNH	2	Contract manufacturer	accessdata.fda.gov
Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis	OSH	2	Contract manufacturer	accessdata.fda.gov
Pin, Fixation, Smooth	HTY	2	Contract manufacturer	accessdata.fda.gov
Plate, Fixation, Bone	HRS	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer	HSN	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer	KWZ	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Femoral Component, Cemented, Metal	JDG	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Hemi-, Femoral, Metal	KWL	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Hemi-, Femoral, Metal Ball	LZY	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented	KWY	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented	LZO	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented	JDI	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented	LPH	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented	LWJ	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate	MEH	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous	MBL	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive	OIY	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer	JWH	2	Contract manufacturer	accessdata.fda.gov
Screw, Fixation, Bone	HWC	2	Contract manufacturer	accessdata.fda.gov
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories	KCT	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Template	HWT	1	Contract manufacturer	accessdata.fda.gov
Thoracolumbosacral Pedicle Screw System	NKB	2	Contract manufacturer	accessdata.fda.gov
Tray, Surgical	LRP	1	Contract manufacturer	accessdata.fda.gov
Tray, Surgical, Instrument	FSM	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Wrap, Sterilization	FRG	2	Contract manufacturer, Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
October 22, 2004	K040223	POLYVAC INSTRUMENT DELIVERY SYSTEM	KCT	Substantially Equivalent	Symmetry Medical USA, Inc.	accessdata.fda.gov
August 2, 2002	K012105	POLYVAC SURGICAL INSTRUMENT DELIVERY SYSTEM	KCT	Substantially Equivalent	Symmetry Medical, Inc.	accessdata.fda.gov
December 7, 2001	K993535	METAPAK MULTI-PURPOSE INSTRUMENT TRAY	FRG	Substantially Equivalent	Riley Medical, Inc.	accessdata.fda.gov
November 22, 1994	K944025	SURGICAL INSTRUMENT TRAY	FSM	Substantially Equivalent	Riley Medical, Inc.	accessdata.fda.gov

Compare with other makers

Updated October 22, 2004. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.