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Data / Medical devices / United States / Stryker Sustainability Solutions - Chandler

Stryker Sustainability Solutions - Chandler: FDA-registered device maker in Chandler, AZ, United States, 30 510(k) clearances

Stryker Sustainability Solutions - Chandler is registered with the FDA (registration 3030153385) in Chandler, AZ, United States. It lists 12 device types. The FDA files 30 510(k) clearances under its listings, the newest dated June 18, 2026. Registered through 2027. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3030153385
Address
6635 W Frye Rd, Chandler, AZ, United States, 85226
Owner or operator
STRYKER CORP. (1811755)
Roles
Remanufacturer, Reprocessor
First device listed
June 20, 2007
Registered through
2027
Brand names listed
LXMJ23L Remanufactured LigaSure XP Maryland Jaw Open Sealer/Divider Latching Handle, Without Nano-coating 5mm - 23cm, LXMJ23S Remanufactured LigaSure XP Maryland Jaw Open Sealer/Divider One-step Sealing, Without Nano-coating 5mm - 23cm, LXMJ37L Remanufactured LigaSure XP Maryland Jaw Laparoscopic Sealer/Divider Latching Handle, Without Nano-coating 5mm -, LXMJ37S Remanufactured LigaSure XP Maryland Jaw Laparoscopic Sealer/Divider One-step Sealing, Without Nano-coating 5mm, LXMJ44L Remanufactured LigaSure XP Maryland Jaw Laparoscopic Sealer/Divider Latching Handle, Without Nano-coating 5mm -, LXMJ44S Remanufactured LigaSure XP Maryland Jaw Laparoscopic Sealer/Divider One-step Sealing, Without Nano-coating 5mm, Remanufactured LigaSure Exact Dissector Without Nano-coating, Remanufactured LigaSure Exact Dissector, Without Nano-coating and more

Devices it lists

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 18, 2026K260636Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coatingGEISubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
August 14, 2025K250898Reprocessed HARMONIC 700 Shears (HAR723/Reprocessed HARMONIC 700, 5mm Diameter Shears with Advanced Hemostasis x 23cm); Reprocessed HARMONIC 700 Shears (HAR736/Reprocessed HARMONIC 700, 5mm Diameter Shears with Advanced Hemostasis x 36cm); Reprocessed HARMONIC 700 Shears (HAR745/Reprocessed HARMONIC 700, 5mm Diameter SHears with Advanced Hemostasis x 45cm)NLQSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
October 22, 2024K241758Reprocessed RD SET Adt Pulse Oximeter Sensor (4000); Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001); Reprocessed RD SET Inf Pulse Oximeter Sensor (4002); Reprocessed RD SET Adt Pulse Oximeter Sensor (4003)NLFSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
July 3, 2024K241606Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm Length (HAR1120); Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 36cm Length (HAR1136)NLQSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
February 20, 2024K233471Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm length (HAR1120); Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 36cm length (HAR1136)NLQSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
March 28, 2023K230255Remanufactured LigaSure Exact Dissector Without Nano-coating LF2019GEISubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
March 28, 2023K230251Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)NUJSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
December 4, 2022K222019Reprocessed RD SET Adt Pulse Oximeter Sensor (4000), Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001), Reprocessed RD SET Inf Pulse Oximeter Sensor (4002), Reprocessed RD SET Adt Pulse Oximeter Sensor (4003)NLFSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
May 25, 2022K220481Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019)GEISubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
May 13, 2022K220411Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)NUJSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
March 8, 2022K211140Reprocessed Masimo Pulse Oximeter (1859 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (1860 Pediatric O2 Transducer), Reprocessed Masimo Pulse Oximeter (1861 Infant O2 Transducer), Reprocessed Masimo Pulse Oximeter (1862 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (2317 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (2319 Infant O2 Transducer), Reprocessed Masimo Pulse Oximeter (2320 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (2328 Infant O2DQASubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
March 8, 2022K211138Reprocessed Pulse Oximeter Sensor (D-25), Reprocessed Pulse Oximeter Sensor (D-25L), Reprocessed Pulse Oximeter Sensor (D-20), Reprocessed Pulse Oximeter Sensor (N-25), Reprocessed Pulse Oximeter Sensor (I-20), Reprocessed Pulse Oximeter Sensor (Max-A), Reprocessed Pulse Oximeter Sensor (Max-AL), Reprocessed Pulse Oximeter Sensor (Max-P), Reprocessed Pulse Oximeter Sensor (Max-N), Reprocessed Pulse Oximeter Sensor (Max-I)NLFSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
March 16, 2021K202554Reprocessed HARMONIC ACE+ 7, 5 mm Diameter Shears with Advanced HemostasisNLQSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
September 25, 2020K201756Reprocessed MyoSure Tissue Removal Device, Reprocessed MyoSure REACH Tissue Removal Device, Reprocessed MyoSure LITE Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device for FluentHIHSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
July 31, 2020K201511Reprocessed Endoscopic Trocars and SleevesNLMSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
April 23, 2018K180499Reprocessed LigaSure Maryland Jaw Sealer/DividerNUJSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
April 20, 2018K180451Reprocessed LigaSure Impact without Nano-coating Large Jaw, Open Sealer/DividerNUJSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
November 16, 2017K172856Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/DividerGEISubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
April 5, 2017K170456Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue TechnologyNLQSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
February 23, 2017K161693Reprocessed HARMONIC ACE+7, 5 mm Diameter Shears with Advanced HemostasisNLQSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
May 1, 2014K133672REPROCESSED HARMONIC ACE SHEARS WITHOUT ADAPTIVE TISSUE TECHNOLOGYNLQSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
April 10, 2014K133578REPROCESSED LIGASURE BLUNT TIP LAPAROSCOPIC SEALER/DIVIDERNUJSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
December 31, 2013K132629REPROCESSED DILATING TIP TROCARSNLMSubstantially EquivalentStryker Sustainability Solutionsaccessdata.fda.gov
July 23, 2010K100909REPROCESSED COMPRESSION SLEEVESJOWSubstantially EquivalentAscent Healthcare Solutionsaccessdata.fda.gov
March 19, 2010K100080REPROCESSED TROCARS, MODEL B5LT AND CB5LTNLMSubstantially EquivalentAscent Healthcare Solutionsaccessdata.fda.gov
July 29, 2008K081238REPROCESSED MASIMO PULSE OXIMETER SENSORSNLFSubstantially EquivalentAscent Healthcare Solutionsaccessdata.fda.gov
January 6, 2005K042316VANGUARD REPROCESSED PULSE OXIMETER SENSORSNLFSubstantially EquivalentVanguard Medical Concepts, Inc.accessdata.fda.gov
October 4, 2002K012344VANGUARD REPROCESSED PULSE OXIMETER SENSORSNLFSubstantially EquivalentVanguard Medical Concepts, Inc.accessdata.fda.gov
November 7, 2001K012635REPROCESSED STRYKER ARTHROSCOPIC SHAVERSHRXSubstantially EquivalentAlliance Medical Corp.accessdata.fda.gov
February 19, 1991K910512ACCUFLATEKCYSubstantially EquivalentInstrumed, Inc.accessdata.fda.gov

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Updated June 18, 2026. 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.