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Data / Medical devices / System, Surgical, Computer Controlled Instrument

System, Surgical, Computer Controlled Instrument (NAY): 48 FDA-registered makers in 11 countries

48 establishments in 11 countries are registered with the FDA to make System, Surgical, Computer Controlled Instrument (product code NAY, Class 2, 21 CFR 876.1500). 13 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 166 510(k) clearances under this code, the latest on September 8, 2026, and lists 113 recall events (2 Class I). FDA data exported November 2, 2026.

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Product code
NAY
Device class
2
Regulation
876.1500
Medical specialty
Gastroenterology, Urology

Makers by country

CountryMakers
United States21
Germany11
Mexico4
Bulgaria2
Dominican Republic2
China2
Israel2
South Korea1
Singapore1
Czechia1
United Kingdom1

Makers of System, Surgical, Computer Controlled Instrument

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Intuitive Surgical, Inc.Sunnyvale, CA, United StatesManufacturer, Manufacturer for export, Specification developer129September 8, 202601111api.fda.gov
Intuitive Surgical, Inc.Santa Clara, CA, United StatesComplaint file establishment, Manufacturer for export129September 8, 2026000api.fda.gov
Intuitive Surgical, Inc.Peachtree Corners, GA, United StatesManufacturer, Remanufacturer, Repackager or relabeler44January 16, 2026000api.fda.gov
Intuitive Surgical, S. de R.L. de C.V.Mexicali Baja California, MexicoExporter to the US, Manufacturer29March 11, 2026000api.fda.gov
Intuitive Surgical, Inc.Sunnyvale, CA, United StatesManufacturer, Manufacturer for export17March 11, 2026000api.fda.gov
Intuitive Surgical, Inc.Sunnyvale, CA, United StatesManufacturer5January 16, 2026000api.fda.gov
AKTORmed GmbHNeutraubling Bavaria, GermanyManufacturer2December 22, 2020000api.fda.gov
Intuitive Surgical Optics GmbHFreiburg Baden-Wurttemberg, GermanyManufacturer2March 14, 2024000api.fda.gov
Intuitive Surgical Optics GmbHEmmendingen Baden-Wurttemberg, GermanyManufacturer2March 14, 2024000api.fda.gov
Intuitive Surgical, Inc.Phoenix, AZ, United StatesManufacturer2March 14, 2024000api.fda.gov
Intuitive Surgical, Inc.Sunnyvale, CA, United StatesManufacturer1March 16, 2023000api.fda.gov
Intuitive Surgical Bulgaria EOODParvomay Plovdiv, BulgariaManufacturer1July 26, 2019000api.fda.gov
Novanta Medical GmbHBerlin, GermanySpecification developer1March 14, 2024000api.fda.gov
Amphenol Alden Products CompanyHermosillo Sonora, MexicoContract manufacturer0000api.fda.gov
Amphenol DC ElectronicsNogales Sonora, MexicoContract manufacturer0000api.fda.gov
Bowa-Electronic GMBHGOMARINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Biomerics NLEMonroe, CT, United StatesContract manufacturer0000api.fda.gov
Das Medical International, SRLLa Romana, Dominican RepublicContract manufacturer0000api.fda.gov
Dongguan Honfield Precision Parts Co., LtdZhangmutou, Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Endorobotics Co., Ltd.Seoul, South KoreaManufacturer0000api.fda.gov
Eurofins STERIPAC GMBHCalw-Altburg Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Fabrinet WestSanta Clara, CA, United StatesContract manufacturer0000api.fda.gov
Fong's Engineering & Manufacturing Private LimitedSingapore Central Singapore, SingaporeContract manufacturer0000api.fda.gov
Guenter Bissinger Medizintechnik GMBHTENINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Humantouch Surgical Ltd.Netanya Central, IsraelComplaint file establishment, Manufacturer0000api.fda.gov
Hupfer Metallwerke GMBH & Co. KGCoesfeld North Rhine-Westphalia, GermanyContract manufacturer0000api.fda.gov
I. ShermanAcre Northern, IsraelContract manufacturer0000api.fda.gov
Koscher & Wuertz GMBHSPAICHINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Linemaster Switch Corp.Woodstock, CT, United StatesContract manufacturer0000api.fda.gov
LISI MEDICAL REmmeleBig Lake, MN, United StatesContract manufacturer0000api.fda.gov
M&L Precision Machining Inc.Morgan Hill, CA, United StatesContract manufacturer0000api.fda.gov
Mass Precision, Inc.Fremont, CA, United StatesContract manufacturer, Manufacturer for export0000api.fda.gov
Microtek Dominicana, S.A.S.Las Americas Santo Domingo, Dominican RepublicContract manufacturer0000api.fda.gov
Norwood Medical LLCDayton, OH, United StatesContract manufacturer0000api.fda.gov
Novanta Medical S.R.O.Prelouc Pardubicky Kraj, CzechiaContract manufacturer0000api.fda.gov
Novanta Medical GmbHLUDWIGSSTADT Bavaria, GermanyContract manufacturer0000api.fda.gov
ORIGAMI SURGICAL Inc.Dover, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
R.K. ManufacturingDanbury, CT, United StatesContract manufacturer0000api.fda.gov
Restore Robotics Repairs LLCHenderson, NV, United StatesRemanufacturer0000api.fda.gov
Samax Precision Inc.Sunnyvale, CA, United StatesContract manufacturer0000api.fda.gov
Schoelly Fiberoptic, GMBHDENZLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Schoelly-Optix OodPanagyurishte Pazardzhik, BulgariaContract manufacturer0000api.fda.gov
SRA Developments LtdKingskerswell Devon, United KingdomContract manufacturer0000api.fda.gov
Supreme Screw ProductsPlainview, NY, United StatesContract manufacturer0000api.fda.gov
Tecan Cdmo Solutions MH, Corp.Morgan Hill, CA, United StatesContract manufacturer0000api.fda.gov
Teleflex Medical de Tecate, S. de R.L de C.V.TECATE Baja California, MexicoContract manufacturer0000api.fda.gov
Veridiam, LLCEl Cajon, CA, United StatesContract manufacturer0000api.fda.gov
Zhuhai Dipu Medical Technology Co., Ltd.Zhuhai Guangdong, ChinaManufacturer0000api.fda.gov

Updated September 8, 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.