# THE ANSPACH EFFORT, INC.

FEI: 1045834
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: THE ANSPACH EFFORT, INC. (#1045834)

Address: 4500 RIVERSIDE DR., Palm Bch Gdns, FL, US



## Products

Total registered: 2
Top product codes: DZI, DZJ
Regulation §: 872.4120

Proprietary names: Synthes

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221045834%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1045834