Atlas FDA

Daavlin Distributing Company

9 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Daavlin Distributing Company

RecordFirmDate
Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders recall (Z-2742-2026)Daavlin Distributing Company2026-07-15
Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders recall (Z-2743-2026)Daavlin Distributing Company2026-07-15
Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders recall (Z-2744-2026)Daavlin Distributing Company2026-07-15
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders suc recall (Z-2295-2026)Daavlin Distributing Company2026-06-02
3 Series Full Body Phototherapy Device with Smart Touch Control System, Models #PASNBSM-24 recall (Z-1233-04)Daavlin Distributing Company2004-07-30
3 Series Full Body Phototherapy Device with Smart Touch Control System, Model All Touch Co recall (Z-1234-04)Daavlin Distributing Company2004-07-30
3 Series Full Body Phototherapy Device with Smart Touch Control System, Model #LNBH-0048. recall (Z-1235-04)Daavlin Distributing Company2004-07-30
3 Series Full Body Phototherapy Device with Smart Touch Control System, Model #SNBSM-0048. recall (Z-1236-04)Daavlin Distributing Company2004-07-30
3 Series Full Body Phototherapy Device with Smart Touch Control System, Model #ANBSM-0048. recall (Z-1237-04)Daavlin Distributing Company2004-07-30

Track Daavlin Distributing Company automatically

Every clearance here is in the API, with alerts when new ones post.