# CORNING-KENNEBUNK

FEI: 1218905
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Corning Incorporated (#1317452)

Address: 2 Alfred Rd, KENNEBUNK, ME, US



## Products

Total registered: 1
Top product codes: FMH
Regulation §: 864.3250

Proprietary names: Falcon Individually Wrapped Round-Bottom Tubes;, Corning Closed Systems individually wrapped centrifuge tubes and accessories, Corning Cryogenic vials and accessories;, Containers

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221218905%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1218905