# Pepin Mfg., Inc.

- Location (FDA's records): Stoughton, WI
- FDA decisions: 3 (1994–2007): 3 510(k) clearances
- Product codes: GZJ (1), EGJ (1), GXY (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 5 (1 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
- Iomed, Inc.: 2 (https://510kreport.com/company/iomed)
- Selectivemed Components, Inc.: 1 (https://510kreport.com/company/selectivemed-components)
- Naimco, Inc.: 1 (https://510kreport.com/company/naimco)
- Lead-Lok, Inc.: 1 (https://510kreport.com/company/lead-lok)
- Uni-Patch, Inc.: 1 (https://510kreport.com/company/uni-patch)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)

## Firms that cite its devices most
- Columbia Scientific Development, LLC: 1 (https://510kreport.com/company/columbia-scientific-development)
- Eletromed, Inc.: 1 (https://510kreport.com/company/eletromed)
- Cathay International, Ltd.: 1 (https://510kreport.com/company/cathay-international)
- Gradient Technologies, LLC: 1 (https://510kreport.com/company/gradient-technologies)

## Its most-cited devices
- K932849: Pmi Tens Electrode (1994), cited by 3
- K070807: Cutaneous Electrotherapy and Recording Electrodes; Tens Electrodes (2007), cited by 2

## Recent decisions
- K070807: Cutaneous Electrotherapy and Recording Electrodes; Tens Electrodes (May 23, 2007)
- K060579: Comfort/IO Iontophoresis Electrodes (Apr 20, 2006)
- K932849: Pmi Tens Electrode (Jan 27, 1994)

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