FDA applicant
Daavlin Distributing Co.
FDA records 18 decisions for Daavlin Distributing Co. (Bryan, OH) from 2002 to 2023: 18 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and ONE (Powered Light Based Non-Laser Surgical…). Since 2016 its 510(k)s took a median of 75 days from receipt to decision, against 88 for FDA’s reviews in the same codes and years. Its devices cite 26 predicates, 15 of them its own earlier devices. 6 recalls are linked to its devices.
FDA’s records also spell it “Daavlin Distributing Company”, “The Daavlin Distributing Company”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Daavlin Distributing Co.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2023
2026 so far, outlined.
Recalls per year
3in 2026
Class I Class II/III not classified
Planning a device like Daavlin Distributing 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 “Daavlin”
FDA records each applicant name separately; these may or may not be the same firm.