Discus Dental, LLC
Discus Dental, LLC holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2010, with 2 FDA device recalls on record.
Top product codes for Discus Dental, LLC
FDA recalls by Discus Dental, LLC
- Z-0425-2015 — Relief ACP Oral Care Gel intended to relieve discomfort from dentin sensitivity. Sold separately in single, single syringe, 4 packs, 6 packs and in teeth whitening kits
- Z-1186-2013 — SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera Street, Culver City CA 90232. The SL3 is a soft-tissue diode laser intended to be used for dental procedures
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Discus Dental, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.