# CENTRON CORPORATION

FEI: 3010773581
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Centron Corporation (#10045761)

Address: 44 Beolmal-ro, Dongan-gu, Anyang-si Gyeonggi, 14059, KR

Mandatory US Agent: CENTROVEST

## Products

Total registered: 1
Top product codes: KSD
Regulation §: 864.9750

Proprietary names: TUBE SEALER SE640, TUBE SEALER SE340, TUBE SEALER SE540, TUBE SEALER SE470RS, TUBE SEALER SE530, TUBE SEALER SE330, TUBE SEALER SE170, TUBE SEALER SE160, TUBE SEALER SE7, TUBE SEALER SE9

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010773581%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010773581