FDA Device Establishments · JSON-LD · Markdown
FEI 2916714 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 2916714 |
|---|---|
| Owner / Operator | AESCULAP, INC. (#2916714) |
| Address | 3773 CORPORATE PKWY., CENTER VALLEY, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | KCT |
| Regulation § (21 CFR) | 880.6850 |
Source: openFDA. Public-domain (CC0).