# Sklar Corp.

- Location (FDA's records): Great Neck, NY
- FDA decisions: 2 (2009–2010): 2 510(k) clearances
- Product codes: KCT (1), FYA (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Miltex, Inc.: 1 (https://510kreport.com/company/miltex)
- Welmed, Inc.: 1 (https://510kreport.com/company/welmed)

## Firms that cite its devices most
- Bahadir USA Corp.: 2 (https://510kreport.com/company/bahadir-usa)
- Ermis Medizintechnik: 1 (https://510kreport.com/company/ermis-medizintechnik)

## Its most-cited devices
- K091720: Sklarlite Rigid Sterilization Container System (2010), cited by 3

## Recent decisions
- K091720: Sklarlite Rigid Sterilization Container System (Apr 9, 2010)
- K082479: Sklar Surgical Gown (Apr 24, 2009)

Source page: https://510kreport.com/company/sklar