# Sds Dental, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 21 (1986–1999): 21 510(k) clearances
- Product codes: EIA (4), FSY (1), HME (1), EAZ (1), EJP (1), BWN (1), KOJ (1), ELC (1), ECB (1), KLC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K990546: Delsonic 2000 (Nov 5, 1999)
- K990545: Jetsonic 2000 (Aug 11, 1999)
- K964619: Delivery System (SDS 1400 XL)/Delivery System Cuspidor (SDS1450,SDS1650 XL) (Jan 22, 1997)
- K902864: Surgical Lighting-Centra 450 (Sep 10, 1990)
- K902865: Baumer Surgical Table (Sep 10, 1990)
- K863011: Dentatus LS/Euroflex F-IV/Isolight Reflect/CM-II (Oct 10, 1986)
- K863007: Euroflex F-IV, Isoflex Iii (Oct 1, 1986)
- K863015: Isoprat C-Iii Set/Isocart Iii Auxiliary Unit (Oct 1, 1986)

Source page: https://510kreport.com/company/sds-dental