# Endoplus

- Location (FDA's records): Mundelein, IL
- FDA decisions: 1 (2015–2015): 1 510(k) clearance
- Product codes: HFI (1)
- Predicates its devices cite: 1 (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 whose devices it cites most
- PAJUNK GmbH Medizintechnologie: 1 (https://510kreport.com/company/pajunk-medizintechnologie)

## Firms that cite its devices most
- Surgical Direct, Inc.: 1 (https://510kreport.com/company/surgical-direct)

## Its most-cited devices
- K151567: ENDOPLUS hand-held laparoscopic instruments (2015), cited by 1

## Recent decisions
- K151567: ENDOPLUS hand-held laparoscopic instruments (Dec 23, 2015)

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