# Hohenstein Enterprises, Inc.

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: KKY (1)
- Predicates its devices cite: 1 (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
- Porex Technologies Corp.: 1 (https://510kreport.com/company/porex-technologies)

## Firms that cite its devices most
- Ceremed, Inc.: 1 (https://510kreport.com/company/ceremed)
- Vivoxid, Ltd.: 1 (https://510kreport.com/company/vivoxid)
- Synthes (USA) Products, LLC: 1 (https://510kreport.com/company/synthes-usa-products)

## Its most-cited devices
- K022665: Porous Hdpe Surgical Implants, to BE Distributed Under Various Trademarks Including Epor, Biopor, Minopor & P-Hdpe (2002), cited by 3

## Recent decisions
- K022665: Porous Hdpe Surgical Implants, to BE Distributed Under Various Trademarks Including Epor, Biopor, Minopor & P-Hdpe (Oct 9, 2002)

Source page: https://510kreport.com/company/hohenstein-enterprises