Not currently registered with FDA under this name

Arthrocare Corp.

Sunnyvale, CA, United States. Named as applicant on 1 dental 510(k) clearance between 1996 and 1996. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11996–1996
Markets registered in
18779 registrations outside the US
Establishments
0—
1996: 11990200020102020

510(k) clearances per year, 1990–2026

Registered in 18 markets

Where regulators' registries name Arthrocare Corp. as the manufacturer or the registration holder of a device.

All markets
United States: 1 clearancesCanada: 345 registrationsSouth Korea: 59 registrationsSaudi Arabia: 47 registrationsUnited Kingdom: 43 registrationsCosta Rica: 39 registrationsTaiwan: 39 registrationsBrazil: 32 registrationsColombia: 32 registrationsAustralia: 27 registrationsSerbia: 25 registrationsPeru: 24 registrationsIsrael: 23 registrationsChina: 19 registrationsHong Kong: 12 registrationsEgypt: 7 registrationsJapan: 5 registrationsEuropean Union: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantArthrocare Corp.1 clearances1996–1996Below
CanadaHealth CanadaRegistration holderARTHROCARE CORPORATION3451999–2026Pure Global AI
South KoreaMFDSManufacturerArthroCare CorporationArthrocare Corporation591999–2026Pure Global AI
Saudi ArabiaSFDAManufacturerArthroCare Corporation47—Pure Global AI
United KingdomMHRAManufacturerArthroCare Corporation43—Pure Global AI
Costa RicaMinisterio de SaludManufacturerARTHROCARE CORPORATION39—Pure Global AI
TaiwanTFDAManufacturerArthroCare CorporationARTHROCARE CORPORATION · ARTHRO CARE CORPORATION391999–2023Pure Global AI
BrazilANVISAManufacturerARTHROCARE CORPORATION322009–2023Pure Global AI
ColombiaINVIMAManufacturerARTHROCARE CORPORATION32—Pure Global AI
AustraliaTGAManufacturerArthrocare Corporation272005–2022Pure Global AI
SerbiaALIMSManufacturerArthroCare Corporation252024–2026Pure Global AI
PeruDIGEMIDManufacturerARTHROCARE CORPORATION242019–2025Pure Global AI
IsraelAMARManufacturerArthroCare CorporationARTHROCARE CORPORATION · Arthrocare Corporation23—Pure Global AI
ChinaNMPARegistration holder美国健尔有限公司ArthroCare Corporation美国健尔有限公司 ArthroCare Corporation19—Pure Global AI
Hong KongMDDManufacturerArthroCare CorporationArthroCare122021–2026Pure Global AI
EgyptEDAManufacturerArthrocare Corporation,72019–2019Pure Global AI
JapanPMDARegistration holderArthroCare Corporation52008–2011Pure Global AI
European UnionEUDAMEDManufacturerArthroCare Corporation1—Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Arthrocare Corp. as the applicant.

Decided510(k)DeviceDevice type
30 Jul 1996K962445ARTHROCARE DENTAL ELECTROSURGERY SYSTEMEKZ Dental Electrosurgical Unit and Accessories

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.