# Lee Pharmaceuticals

- Location (FDA's records): Mchenry, IL
- FDA decisions: 29 (1976–1993): 29 510(k) clearances
- Product codes: EBF (8), KLE (5), DYH (5), EJJ (2), EBC (2), DZS (2), DYW (1), EBD (1), EBZ (1), EID (1), KIF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Nordiska Dental AB: 1 (https://510kreport.com/company/nordiska-dental)

## Its most-cited devices
- K912256: Precise (R) Beta Quartz Glass-Ceramic Insert (1991), cited by 1

## Recent decisions
- K924378: Restobond 4 (Mar 31, 1993)
- K912256: Precise (R) Beta Quartz Glass-Ceramic Insert (Jul 24, 1991)
- K900809: Lee-Fischer Ceramic Reinforced Plastic Brackets (Jun 28, 1990)
- K894315: Restobond 3/Dentin-Enamel Bonding Agent (Oct 31, 1989)
- K881903: Prosthodent VL (Jul 1, 1988)
- K873123: Lee Composite Inlay System (Jan 20, 1988)
- K863157: Restodent Posterior (Sep 25, 1986)
- K854882: Protec/Visible Light-Cured Sealant/Dental Restorat (Jan 30, 1986)

Source page: https://510kreport.com/company/lee-pharmaceuticals