FDA applicant
Rhodia, Inc.
FDA records 3 decisions for Rhodia, Inc. (Ventura, CA) from 2001 to 2002: 3 510(k) clearances. All are in product code ELW (Material, Impression). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Rhodia, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Rhodia, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Rhodia, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report