# Stryker Corp. > Medical device manufacturer record on deviCERTS, compiled from public registries. Stryker Corp. is a medical device manufacturer, with 14,690 devices listed and 683 FDA recalls as of 14 Nov 2026. - Canonical page: - Also registered as: Stryker; Stryker Corporation - Country: United States (from the FDA registration address) - Role: Manufacturer, Part of a group - Registrations: FDA - FDA FEI: 1811755 ## Figures - Devices: 14,690 - FDA recalls (matched to the firm by name): 683, 108 ongoing (4 open since before 2021) ## Registry facts *The 3,000 best-ranked devices of 14,690.* - Registries: FDA GUDID 2,998, EUDAMED 1,474, FDA 510(k) 2 - Device classes: FDA Class II 1,791, FDA Class I 1,126, FDA Unclassified 49, FDA Class III 29 ## Sites and related companies - Part of [Stryker GmbH](https://devicerts.com/manufacturers/stryker-gmbh) ## Devices The first 50 of 14,690, in the order of the canonical page, which lists them all. - [Excelsior Reach MC17PSJ155-01](https://devicerts.com/devices/excelsior-reach-mc17psj155-01) · Class II · GUDID · status: Active - [Excelsior Reach MC17PS90155-01](https://devicerts.com/devices/excelsior-reach-mc17ps90155-01) · Class II · GUDID · status: Active - [Excelsior Reach MC17PS45165-01](https://devicerts.com/devices/excelsior-reach-mc17ps45165-01) · Class II · GUDID · status: Active - [Excelsior Reach MC17ST155-01](https://devicerts.com/devices/excelsior-reach-mc17st155-01) · Class II · GUDID · status: Active - [Excelsior Reach MC17PS90165-01](https://devicerts.com/devices/excelsior-reach-mc17ps90165-01) · Class II · GUDID · status: Active - [Excelsior Reach MC17PS45155-01](https://devicerts.com/devices/excelsior-reach-mc17ps45155-01) · Class II · GUDID · status: Active - [Excelsior Reach MC17ST165-01](https://devicerts.com/devices/excelsior-reach-mc17st165-01) · Class II · GUDID · status: Active - [Excelsior Reach MC17PSJ165-01](https://devicerts.com/devices/excelsior-reach-mc17psj165-01) · Class II · GUDID · status: Active - [Broadway 8 BRW084128-01](https://devicerts.com/devices/broadway-8-brw084128-01) · Class II · GUDID · status: Active - [Sonopet iQ+ 5500260000](https://devicerts.com/devices/sonopet-iq-5500260000-5500-260-000) · Unclassified · GUDID · status: Listed - [Sonopet iQ 5700050000](https://devicerts.com/devices/sonopet-iq-5700050000-5700-050-000) · Unclassified · GUDID · status: Listed - [Sonopet iQ+ 550026B010](https://devicerts.com/devices/sonopet-iq-550026b010-5500-26b-010) · Unclassified · GUDID · status: Listed - [Sonopet iQ+ 550026B020](https://devicerts.com/devices/sonopet-iq-550026b020-5500-26b-020) · Unclassified · GUDID · status: Listed - [Sonopet iQ+ 550026B114](https://devicerts.com/devices/sonopet-iq-550026b114-5500-26b-114) · Unclassified · GUDID · status: Listed - [Sonopet iQ+ 550026B312](https://devicerts.com/devices/sonopet-iq-550026b312-5500-26b-312) · Unclassified · GUDID · status: Listed - [Sonopet iQ+ 550026B328](https://devicerts.com/devices/sonopet-iq-550026b328-5500-26b-328) · Unclassified · GUDID · status: Listed - [Neptune 0703146005](https://devicerts.com/devices/neptune-0703-146-005) · Class II · EUDAMED, GUDID · status: Active - [Rps 8800050000](https://devicerts.com/devices/rps-8800-050-000) · Class II · GUDID · status: Listed - [Rps 8808000000](https://devicerts.com/devices/rps-8808-000-000) · Class II · GUDID · status: Listed - [5027500100](https://devicerts.com/devices/n-a-5027-500-100) · Class II · GUDID · status: Listed - [5027500000](https://devicerts.com/devices/n-a-5027-500-000) · Class II · GUDID · status: Listed - [5027500200](https://devicerts.com/devices/n-a-5027-500-200) · Class I · GUDID · status: Listed - [Rps 8800055000](https://devicerts.com/devices/rps-8800-055-000) · Class II · GUDID · status: Listed - [Rps 8800004000](https://devicerts.com/devices/rps-8800-004-000) · Class II · GUDID · status: Listed - [Rps 8800511000](https://devicerts.com/devices/rps-8800-511-000) · Class I · GUDID · status: Listed - [Rps 8800513000](https://devicerts.com/devices/rps-8800-513-000) · Class I · GUDID · status: Listed - [Rps 8800512000](https://devicerts.com/devices/rps-8800-512-000) · Class I · GUDID · status: Listed - [5027500400](https://devicerts.com/devices/n-a-5027-500-400) · Class II · GUDID · status: Listed - [Maistro 0620002000](https://devicerts.com/devices/maistro-0620-002-000) · Class I · GUDID · status: Withdrawn - [InZone IST IST345100960](https://devicerts.com/devices/inzone-ist-ist345100960) · Class II · EUDAMED, GUDID · status: Active - [7900132000](https://devicerts.com/devices/na-7900-132-000) · Class I · EUDAMED, GUDID · status: Active - [7900131000](https://devicerts.com/devices/na-7900-131-000) · Class I · EUDAMED, GUDID · status: Active - [7900125000](https://devicerts.com/devices/na-7900-125-000) · Class I · EUDAMED, GUDID · status: Active - [7900062000](https://devicerts.com/devices/na-7900-062-000) · Class I · EUDAMED, GUDID · status: Active - [7900126000](https://devicerts.com/devices/na-7900-126-000) · Class I · EUDAMED, GUDID · status: Active - [Rps 8825185075](https://devicerts.com/devices/rps-8825-185-075) · Class II · GUDID · status: Listed - [VersiQuad 0234112611](https://devicerts.com/devices/versiquad-234-112-611) · Class I · GUDID · status: Listed - [VersiQuad 0234112012](https://devicerts.com/devices/versiquad-234-112-012) · Class I · GUDID · status: Listed - [VersiQuad 0234112109](https://devicerts.com/devices/versiquad-234-112-109) · Class I · GUDID · status: Listed - [VersiQuad 0234112100](https://devicerts.com/devices/versiquad-234-112-100) · Class I · GUDID · status: Listed - [VersiQuad 0234112609](https://devicerts.com/devices/versiquad-234-112-609) · Class I · GUDID · status: Listed - [VersiQuad 0234112600](https://devicerts.com/devices/versiquad-234-112-600) · Class I · GUDID · status: Listed - [VersiQuad 0234112500](https://devicerts.com/devices/versiquad-234-112-500) · Class I · GUDID · status: Listed - [VersiQuad 0234112108](https://devicerts.com/devices/versiquad-234-112-108) · Class I · GUDID · status: Listed - [VersiQuad 0234112607](https://devicerts.com/devices/versiquad-234-112-607) · Class I · GUDID · status: Listed - [VersiQuad 0234112110](https://devicerts.com/devices/versiquad-234-112-110) · Class I · GUDID · status: Listed - [VersiQuad 0234112608](https://devicerts.com/devices/versiquad-234-112-608) · Class I · GUDID · status: Listed - [VersiQuad 0234112610](https://devicerts.com/devices/versiquad-234-112-610) · Class I · GUDID · status: Listed - [SportSuite 0203-1000](https://devicerts.com/devices/sportsuite-0203-1000) · Class II · GUDID · status: Active - [7200015270](https://devicerts.com/devices/n-a-7200-015-270) · Class I · EUDAMED, GUDID · status: Active ## FDA recalls (matched by name, newest first) - Z-2827-2026 · Class II · Ongoing · initiated 2026-07-01 · product code KTT: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Z-2828-2026 · Class II · Ongoing · initiated 2026-07-01 · product code KTT: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Z-2829-2026 · Class II · Ongoing · initiated 2026-07-01 · product code KTT: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Z-2830-2026 · Class II · Ongoing · initiated 2026-07-01 · product code KTT: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Z-2831-2026 · Class II · Ongoing · initiated 2026-07-01 · product code KTT: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Z-2832-2026 · Class II · Ongoing · initiated 2026-07-01 · product code KTT: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Z-2833-2026 · Class II · Ongoing · initiated 2026-07-01 · product code KTT: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Z-2862-2026 · Class II · Ongoing · initiated 2026-06-08 · product code GCX: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - Z-2863-2026 · Class II · Ongoing · initiated 2026-06-08 · product code GCX: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - Z-2864-2026 · Class II · Ongoing · initiated 2026-06-08 · product code GCX: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - Z-2865-2026 · Class II · Ongoing · initiated 2026-06-08 · product code GEI: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - Z-2866-2026 · Class II · Ongoing · initiated 2026-06-08 · product code GEI: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - Z-2282-2026 · Class II · Ongoing · initiated 2026-05-06 · product code JCX: It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable. - Z-2166-2026 · Class II · Ongoing · initiated 2026-04-09 · product code HIG: Due to nonconforming products being inadvertently distributed. - Z-1427-2026 · Class II · Ongoing · initiated 2026-01-21 · product code NEU: Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures. - Z-0599-2026 · Class II · Ongoing · initiated 2025-10-31 · product code GEI: Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction. - Z-0600-2026 · Class II · Ongoing · initiated 2025-10-31 · product code GEI: Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction. - Z-0601-2026 · Class II · Ongoing · initiated 2025-10-31 · product code GEI: Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction. - Z-2277-2025 · Class II · Ongoing · initiated 2025-07-02 · product code KCY: Tourniquet cuff flange may become detached from the bladder. If leak occurs during the procedure, there may be risk of hemorrhage, resulting in blood loss greater than expected. Other serious risks include cerebral hypotension and cardiovascular collapse and arrest, risking stroke or death. Specific to IVRA, patient toxicity may also occur due to rapid systemic absorption of anesthetics. - Z-2170-2025 · Class II · Ongoing · initiated 2025-06-18 · product code GCJ: Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction. - Z-2171-2025 · Class II · Ongoing · initiated 2025-06-18 · product code GCX: Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction. - Z-1914-2025 · Class II · Ongoing · initiated 2025-05-28 · product code HSB: Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail. - Z-1939-2025 · Class II · Ongoing · initiated 2025-05-22 · product code HSB: Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail. - Z-1940-2025 · Class II · Ongoing · initiated 2025-05-22 · product code HSB: Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail. - Z-1620-2025 · Class II · Ongoing · initiated 2025-03-28 · product code LXH: The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. ## Source and citation - Cite as: Stryker Corp. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/stryker-corp (data as of 2026-11-14). - Data sources: [FDA GUDID](https://accessgudid.nlm.nih.gov/), [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm), [FDA recalls](https://open.fda.gov/apis/device/recall/) - FDA recall data as of: 2026-11-01 - Data as of: 2026-11-14 - JSON: - Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms. - Attribution: DevicErts, https://devicerts.com/manufacturers/stryker-corp - Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.