# Satelec - Acteon Group

- Location (FDA's records): Mt. Laurel, NJ
- FDA decisions: 11 (2007–2024): 11 510(k) clearances
- Product codes: ELC (7), DZI (2), EBZ (1), EBW (1)
- Predicates its devices cite: 17 (6 its own); citations of its devices by later devices: 8 (6 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
- Satelec: 8 (https://510kreport.com/company/satelec)
- Ivoclar Vivadent, Inc.: 1 (https://510kreport.com/company/ivoclar-vivadent)
- Satelec - Acteon, Inc.: 1 (https://510kreport.com/company/satelec-acteon)
- Dentsply International, Inc.: 1 (https://510kreport.com/company/dentsply-international)

## Firms that cite its devices most
- Satelec: 1 (https://510kreport.com/company/satelec)
- Nakanishi, Inc.: 1 (https://510kreport.com/company/nakanishi)

## Its most-cited devices
- K113430: Proultra Piezo Ultrasonic (2012), cited by 3
- K071424: Pmax Newtron XS (2007), cited by 2
- K233922: SP Newtron Can-a; Module Newtron Can-a Emb; Support Xinetic; NWT Can Slim Led Cord G3 Short; NWT Can Slim Led Cord G3 Long (2024), cited by 1
- K072030: Implant Center (2007), cited by 1
- K111623: I-Endo Dual (2012), cited by 1

## Recent decisions
- K233922: SP Newtron Can-a; Module Newtron Can-a Emb; Support Xinetic; NWT Can Slim Led Cord G3 Short; NWT Can Slim Led Cord G3 Long (Mar 11, 2024)
- K172137: Piezotome Cube (May 3, 2018)
- K131906: Scanwave Pen (with Light Gray Cord), Scanwave Pen (with Medium Gray Cord), Scanwave Pen (with Dark Gray Cord), Scanwave (Apr 11, 2014)
- K132322: Newtron P5 XS B.Led (Mar 11, 2014)
- K132267: Newtron P5, Newtron P5 B.Led (Mar 10, 2014)
- K131151: Endocenter (Jan 16, 2014)
- K131997: Newtron Booster (Nov 26, 2013)
- K113430: Proultra Piezo Ultrasonic (Feb 23, 2012)

Source page: https://510kreport.com/company/satelec-acteon-group