# Pentron Laboratory Technologies

- Location (FDA's records): Wallingford, CT
- FDA decisions: 5 (2002–2003): 5 510(k) clearances
- Product codes: EBF (2), EJH (2), EJT (1)
- Predicates its devices cite: 4 (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

## Firms whose devices it cites most
- Jeneric/Pentron, Inc.: 4 (https://510kreport.com/company/jeneric-pentron)

## Recent decisions
- K023742: Sculpture Plus Nano-Hybrid Composite (Jan 17, 2003)
- K023499: Gold Core Plus (Jan 13, 2003)
- K023501: Gold Core 35 (Dec 18, 2002)
- K023502: Jewel Cast Plus (Dec 18, 2002)
- K020555: Sonata Micro Hybrid Composite (Apr 22, 2002)

Source page: https://510kreport.com/company/pentron-laboratory-technologies