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MAKO Surgical Corp.

United States·US-MF-000000703

Last updated September 17, 2026

What MAKO Surgical Corp. makes

MAKO Surgical Corp. manufactures orthopedic surgical devices including unicondylar knee prostheses, knee tibia prosthesis trials (reusable), uncoated unicondylar knee tibia prostheses made of polyethylene, non-constrained polyethylene acetabular liners, surgical implant templates (reusable), instrument trays (reusable), knee femur prosthesis trials (reusable), and metallic femoral head prostheses. The company also produces irrigation clips, orthopedic prosthesis instruments, reamers and burs, software discs, and devices under the RESTORIS and VIZADISC product lines, such as RESTORIS ESYNTIAL.

These devices are classified as Class I, Class II, and Class IIa medical devices and are listed in the EUDAMED and FDA UDI registries. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does MAKO Surgical Corp. manufacture?

MAKO Surgical Corp. manufactures orthopedic surgical devices such as unicondylar knee prostheses, reusable knee tibia prosthesis trials, uncoated unicondylar knee tibia prostheses made of polyethylene, non-constrained polyethylene acetabular liners, reusable surgical implant templates, reusable instrument trays, reusable knee femur prosthesis trials, metallic femoral head prostheses, irrigation clips, orthopedic prosthesis instruments, reamers and burs, software discs, and devices under the RESTORIS and VIZADISC product lines, including RESTORIS ESYNTIAL.

Where is MAKO Surgical Corp. based?

MAKO Surgical Corp. is based in the United States, as stated in the provided device data under the COUNTRY field.

Which registries list MAKO Surgical Corp.'s devices?

MAKO Surgical Corp.'s devices are listed in the EUDAMED and FDA UDI registries, as specified in the LISTED IN field of the device data.

How are MAKO Surgical Corp.'s devices classified?

MAKO Surgical Corp.'s devices are classified as Class I, Class II, and Class IIa medical devices, according to the DEVICE CLASSES field in the provided data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: United States
Address: 3365, Enterprise Avenue, Weston, United States
Website: www.stryker.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1 954 927 2044
PRRC Contact: Krutanjali Shah
EUDAMED SRN: US-MF-000000703
FDA FEI Number: 3005985723
DUNS Number: —

Catalogue (874)

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Device	Model / Reference	Registries	Class	Status
Restoris Xlve	186436-58	FDA UDI	Class II	Active
Restoris	186005-35	FDA UDI	Class II	Active
Restoris	180708-8	FDA UDI	Class II	Active
Restoris	160115	FDA UDI	Class II	Active
Restoris	180704-5	FDA UDI	Class II	Active
Makoplasty	150103	FDA UDI	Class I	Active
Mako	1025-200-075	FDA UDI	Class II	Active
Restoris	170702-8	FDA UDI	Class II	Active
Restoris Xlve	186328-48	FDA UDI	Class II	Active
Restoris Esyntial	180743-9	FDA UDI	Class II	Active
Restoris Esyntial	180747-6	FDA UDI	Class II	Active
Restoris	120209-5	FDA UDI	Class II	Active
Restoris Esyntial	180741-1	FDA UDI	Class II	Active
Restoris	180721-1	FDA UDI	Class II	Active
Restoris Esyntial	180744-5	FDA UDI	Class II	Active
Restoris	111541-1	FDA UDI	Class II	Active
Restoris	170504	FDA UDI	Class II	Active
Mako	TKA 1.0.3 + THA 4.0.2 + PKA 3.0.4	FDA UDI	Class II	Active
Restoris	170702-7	FDA UDI	Class II	Active
Rio	112220	FDA UDI	Class II	Active
Restoris	170612	FDA UDI	Class II	Active
Restoris	180728-4	FDA UDI	Class II	Active
Mako	180731-5	FDA UDI	Class II	Active
Restoris	180702-2	FDA UDI	Class II	Active
Rio	111690	FDA UDI	Class II	Active
Makoplasty	151102	FDA UDI	Class I	Active
Accolade Ii	210433-3227	FDA UDI	Class II	Active
Restoris	180724-1	FDA UDI	Class II	Active
Restoris Xlve	186436-56	FDA UDI	Class II	Active
Mako	180732-1-E	FDA UDI	Class II	Active
Restoris	160108	FDA UDI	Class II	Active
Mako	180734-2-E	FDA UDI	Class II	Active
Restoris	160144	FDA UDI	Class II	Active
Stryker	151080	FDA UDI	Class I	Active
Restoris	180701-7	FDA UDI	Class II	Active
Restoris	160146	FDA UDI	Class II	Active
Restoris	180512	FDA UDI	Class II	Active
Restoris	186636-00	FDA UDI	Class II	Active
Restoris	180722-5	FDA UDI	Class II	Active
Restoris	170607	FDA UDI	Class II	Active
Restoris	120209-4	FDA UDI	Class II	Active
Restoris	186040-01	FDA UDI	Class II	Active
Restoris	186036-03	FDA UDI	Class II	Active
Mako	180735-2	FDA UDI	Class II	Active
Restoris Esyntial	180746-7	FDA UDI	Class II	Active
Restoris	180725-4	FDA UDI	Class II	Active
Restoris	160152	FDA UDI	Class II	Active
Restoris	186003-12	FDA UDI	Class II	Active
Mako	180735-2-E	FDA UDI	Class II	Active
Restoris Xlve	186436-62	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Recalls (31)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

There are 31 recall records for MAKO Surgical Corp., with the earliest initiated on 2008-05-02 and the most recent on 2022-08-08. The statuses of these recalls include completed, open, classified, and terminated. The reasons given for the recalls include damaged locking pins during assembly, intermittent electrical problems due to loose screw connections, communication-connection errors, out-of-tolerance components, ungreased bearings on saw attachments, compromised sterile barrier in packaging, software discrepancies in displaying EE constants, potential for infant failures leading to non-functionality or error lights, field manual revisions, potential failure during use causing inaccuracy, damage to Vizadisc reflective material affecting camera detection, and missing AFMEA Risk Control Measures in user guides.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Aug 8, 2022	Z-1735-2022	—	open, classified	Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.
Oct 23, 2020	Z-0472-2021	—	completed	Stryker has discovered a characterization issue associated with the Mako Integrated Cutting System (MICS) Handpiece. The MICS Handpiece is attached to the distal end of the robotic arm and is used to register the RIO and to execute bone preparation during a Mako Total Knee or Mako Partial Knee procedure (PKA Software Application 3.0 or later). This issue may result in unsuccessful checkpoint verification when the Mako System attempts to verify the location of the saw blade prior to bone preparation. This issue may also cause a discrepancy during bone preparation in a Mako Total Knee or a Mako Partial Knee procedure in which the surgeon uses a straight or angled saw attachment with the MICS Handpiece. The surgeon may make cuts during bone preparation that differ from the surgeon s preoperative plan.
Jul 9, 2020	Z-2745-2020	—	terminated	Characterization issue associated with the product. This issue may cause a discrepancy during bone preparation in certain Mako Total Hip procedures.
Apr 25, 2019	Z-1824-2019	—	terminated	The bearings of the saw attachments were ungreased.
Apr 25, 2019	Z-1823-2019	—	terminated	The bearings of the saw attachments were ungreased.
Jul 24, 2018	Z-2925-2018	—	terminated	Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip Procedure Tracking Kit have the potential to be damaged on the Vizadisc reflective material causing an inability to be detected by the camera.
Jul 24, 2018	Z-2924-2018	—	terminated	Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip Procedure Tracking Kit have the potential to be damaged on the Vizadisc reflective material causing an inability to be detected by the camera.
May 10, 2018	Z-2794-2018	—	terminated	Out of tolerance.
Jan 19, 2018	Z-2051-2018	—	terminated	Possible hinge pin disassociation from the Mako Onlay Insert Extractor.
Dec 27, 2017	Z-3182-2018	—	terminated	Communication-connection error.
Dec 1, 2017	Z-1644-2018	—	terminated	Incorrect product and/or label. Sizing is labeled incorrectly.
Aug 7, 2017	Z-3131-2017	—	terminated	Software discrepancy of not showing all the EE constants, when the screen is filled.
Aug 7, 2017	Z-3130-2017	—	terminated	Software discrepancy of not showing all the EE constants, when the screen is filled.
Jun 7, 2017	Z-2741-2017	—	terminated	An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
Dec 22, 2016	Z-1411-2017	—	terminated	Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA Application User Guides
Sep 29, 2016	Z-1193-2017	—	terminated	Failure of the Offset Cup Reamer Handle not engaging its mating components.
Feb 23, 2016	Z-1583-2016	—	terminated	Potential disassociation of the orientation pin.
Jan 15, 2016	Z-1031-2016	—	terminated	Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the clamshell packaging configuration exhibited damage, compromising the sterile barrier.
Nov 25, 2015	Z-1588-2016	—	terminated	Stryker Orthpaedics became aware that there is the potential for the 210540 MAKOplasty Hip Array Kit Laminate 150230 to list two part numbers for the RIO Base Array, which is item #5 on the product table.
Jul 16, 2015	Z-0224-2016	—	terminated	The locking pin on the RIO Base Array is damaged during assembly onto the RIO Base Array Connector.
Jan 22, 2015	Z-1128-2015	—	terminated	When using the MAKOplasty partial knee Arthroplasty application, the burr continues spinning outside of the stereotactic boundary and after the control switches (foot pedal and trigger) cease to be activated
Oct 7, 2014	Z-0830-2015	—	terminated	MAKO has identified the potential that the shell impactors may be damaged intraoperatively.
Oct 7, 2014	Z-0828-2015	—	terminated	MAKO has identified the potential that the shell impactors may be damaged intraoperatively.
Oct 7, 2014	Z-0829-2015	—	terminated	MAKO has identified the potential that the shell impactors may be damaged intraoperatively.
Apr 30, 2014	Z-1508-2016	—	terminated	Revision of the field manual
Jan 9, 2014	Z-1132-2014	—	terminated	The product may be mislabeled and could result in the incorrect implant being used.
Sep 12, 2012	Z-0385-2013	—	terminated	MAKO Surgical Group recalled their RIO System software, version 2.4 and is implementing software version 2.5 to address a software functional issue with the existing version of the system's software. Loss of tactile feedback constraining the cutting burr has been reported.
Jan 20, 2011	Z-0146-2012	—	terminated	MAKO Surgical Corp. is recalling their RIO Robotic Arm Interactive Orthopedic System (RIO) due to software issue that exist that could potentially result in a bone resection. No adverse events reported.
Oct 25, 2010	Z-2232-2011	—	terminated	MAKO Surgical Corporation recalled ONE infra-red camera MAKO PN 204854 which was a component of their RIO Robotic Arm Interactive Orthopedic System with SSN P7-03127, on November 22, 2010. This component can function improperly and cause the accuracy of the system to be outside of the specification listed by the manufacturer. The recall was initiated after the camera manufacture, NDI, Waterloo, On
Jul 17, 2009	Z-0064-2010	—	terminated	Cables fail to provide adequate transmission. MAKO Surgical Corporation is recalling 200996 Cable Assembly, Hybrid Extended Length; 200997 Cable Assembly, Hybrid, Guidance Module; and 200998 Cable Assembly, Hybrid, UI Panel. These parts are sub components of the 20300 Rio Standard System.
May 2, 2008	Z-0915-2009	—	terminated	The product in its current state may fail during use, which would cause the instrument to be in-accurate.