# Paladin Medical, Inc.

- Location (FDA's records): Stillwater, MN
- FDA decisions: 14 (1992–1999): 14 510(k) clearances
- Product codes: HET (8), FMW (1), HRX (1), DTE (1), HAM (1), LYL (1), LLZ (1)
- Predicates its devices cite: 3 (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
- American Pacemaker Corp.: 1 (https://510kreport.com/company/american-pacemaker)
- Bio-Detek, Inc.: 1 (https://510kreport.com/company/bio-detek)
- Surgicad Corp.: 1 (https://510kreport.com/company/surgicad)

## Firms that cite its devices most
- Leonhard Lang GmbH: 1 (https://510kreport.com/company/leonhard-lang)
- Endius, Inc.: 1 (https://510kreport.com/company/endius)
- Autolens, Inc.: 1 (https://510kreport.com/company/autolens)

## Its most-cited devices
- K950054: Endo-Bend (TM) Shaver (1995), cited by 1
- K993306: Nikopad Electrosurgical Grounding Pad (*or Sold Under Commercial Names), Model 4760 (Typically) (1999), cited by 1
- K964222: Acu-Clens Cleaning System for Contact Lens Cleaning (1996), cited by 1

## Recent decisions
- K993306: Nikopad Electrosurgical Grounding Pad (*or Sold Under Commercial Names), Model 4760 (Typically) (Nov 3, 1999)
- K970347: MPC (Model 7000) External Temporary Pacemaker System (Aug 29, 1997)
- K971290: Stratasys FDM Medmodeler System (Jun 20, 1997)
- K964222: Acu-Clens Cleaning System for Contact Lens Cleaning (Dec 20, 1996)
- K950054: Endo-Bend (TM) Shaver (Jun 29, 1995)
- K935220: Core Prevent Mattress Modification (Nov 29, 1993)
- K921015: Sharpe Endosponge Aspiirator (May 21, 1993)
- K915743: Sharpe Endotenaculum (May 20, 1993)

Source page: https://510kreport.com/company/paladin-medical