Manufacturer registered with FDA

ConMed CORP.

Largo, FL, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.

FDA owner/operator1317214Manufacturer
Device types listed
1
Brands and models
1
510(k) clearances
22003–2006
Markets registered in
7578 registrations outside the US
Establishments
1United States
2003: 12006: 1200020102020

510(k) clearances per year, 2000–2026

Registered in 7 markets

Where regulators' registries name ConMed CORP. as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedTaiwan: 148 registrationsColombia: 123 registrationsPeru: 115 registrationsSouth Korea: 106 registrationsBrazil: 69 registrationsIsrael: 17 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerConMed CORP.2 clearances2003–2006Below
TaiwanTFDAManufacturerCONMED CORPORATIONLINVATEC CORPORATION1481994–2026Pure Global AI
ColombiaINVIMAManufacturerCONMED CORPORATION123—Pure Global AI
PeruDIGEMIDManufacturerCONMED CORPORATION1152013–2026Pure Global AI
South KoreaMFDSManufacturerLinvatec CorporationLINVATEC CORPORATION · Linvatec corporation · +21061998–2008Pure Global AI
BrazilANVISAManufacturerCONMED CORPORATIONLINVATEC CORPORATION692009–2022Pure Global AI
IsraelAMARManufacturerConmed CorporationConMed Corporation · Conmed Co. · +217—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

Devices listed with FDA

What ConMed CORP. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Powered Bone DrillDZI · Class 2Surgical drills & motorsMaker
PowerPro Pneumatic
2014

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names ConMed CORP. as the applicant, including filings under its other names.

Decided510(k)DeviceDevice type
10 Apr 2006K060270MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILLDZI Powered Bone Drill
10 Nov 2003K032607POWERPRO PNEUMATIC SYSTEM, MODELS PRO6150, PRO6175, PRO6185DZI Powered Bone Drill

Registered establishments

EstablishmentLocationWhat it does
Linvatec CorporationFDA reg. 1017294LARGO, FL, United StatesManufacturer

Other names on FDA records

Linvatec Corporation

Sources

FDA establishment registration & device listing (search FDA, owner/operator 1317214). 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.