FDA applicant
Charles Atkins & Co.
FDA records 2 decisions for Charles Atkins & Co. (Atlanta, GA) from 1985 to 1986: 2 510(k) clearances. All are in product code HMT (Drape, Patient, Ophthalmic). 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 Charles Atkins & Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Charles Atkins & Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Charles Atkins & Co.’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 “Charles”
FDA records each applicant name separately; these may or may not be the same firm.