# ANCLOTE MANUFACTURING COMPANY

FEI: 3045526569
Status: Active
Establishment types: Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Anclote Manufacturing Company (#10095980)

Address: 12580 Enterprise Blvd Ste A, Largo, FL, US



## Products

Total registered: 1
Top product codes: ISS
Regulation §: 890.3420

Proprietary names: AK Auto Expulsion Valve (VAER), Anclote Vented Distal Cusions (DCSP), Anclote Elevated Vacuum Pump (AEVP), Anclote Suction Plate (PSSP,PSTH), FlexForm (FISP) Flexible Inner Socket

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223045526569%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3045526569