FDA applicant
Aesthetic and Reconstructive Technologies, Inc.
FDA records 10 decisions for Aesthetic and Reconstructive Technologies, Inc. (Paso Robles, CA) from 2002 to 2003: 10 510(k) clearances. Most are in product codes MIB (Elastomer, Silicone Block) and FWP (Prosthesis, Chin, Internal). 6 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Aesthetic and Reconstructive Technologies, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Aesthetic and Reconstructive Technologies, Inc. since 2007.
Recalls per year
6in 2025
Class I Class II/III not classified
Planning a device like Aesthetic and Reconstructive…’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 “Aesthetic”
FDA records each applicant name separately; these may or may not be the same firm.