FDA applicant
Robert W. Bauer & Assoc., Inc.
FDA records 3 decisions for Robert W. Bauer & Assoc., Inc. (Chicago, IL) from 1994 to 1995: 3 510(k) clearances. Most are in product codes ELW (Material, Impression) and EBF (Material, Tooth Shade, Resin). 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 Robert W. Bauer & Assoc., Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Robert W. Bauer & Assoc., Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Robert W. Bauer & Assoc., 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) ReportOther applicant names beginning “Robert”
FDA records each applicant name separately; these may or may not be the same firm.