# J. Sklar Mfg. Co., Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 18 (1977–1984): 18 510(k) clearances
- Product codes: HFB (3), HNF (3), KOA (2), FZT (2), HCZ (1), BTA (1), HGN (1), HGC (1), LKF (1), GEN (1), HTZ (1), HCF (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: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medinvents: 1 (https://510kreport.com/company/medinvents)

## Its most-cited devices
- K842112: Tischler Cervical Biopsy Punch Forceps (1984), cited by 1

## Recent decisions
- K843693: Jacobs High Vacuum Suction Unit 05-2570 (Oct 31, 1984)
- K842112: Tischler Cervical Biopsy Punch Forceps (Jul 3, 1984)
- K842111: Kogan Endospeculum 9-1/2 (Jun 19, 1984)
- K822448: Scissors, Various (Sep 14, 1982)
- K802458: Kevorkian-Younge Biopsy Curette #90-6611 (Jan 12, 1981)
- K802457: Kevorkian-Younge Biopsy Punch, #90-6610 (Jan 12, 1981)
- K801273: Magill Catheter Intro. Forceps (Jul 28, 1980)
- K800441: Rudd-Clinic Hemorrhoidal Forceps (Apr 8, 1980)

Source page: https://510kreport.com/company/j-sklar-mfg