# Oroscience, Inc.

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 2 (2008–2009): 2 510(k) clearances
- Product codes: EMA (1), GEX (1)
- Predicates its devices cite: 8 (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
- Laser Dental Innovations: 2 (https://510kreport.com/company/laser-dental-innovations)
- Coe Laboratories, Inc.: 1 (https://510kreport.com/company/coe-laboratories)
- Hager Worldwide, Inc.: 1 (https://510kreport.com/company/hager-worldwide)
- Quanta System Spa: 1 (https://510kreport.com/company/quanta-system)
- Hoya Conbio, Inc.: 1 (https://510kreport.com/company/hoya-conbio)
- Biolitec, Inc.: 1 (https://510kreport.com/company/biolitec)
- B&W Tek, Inc.: 1 (https://510kreport.com/company/b-w-tek)

## Firms that cite its devices most
- Emanate Biomedical: 1 (https://510kreport.com/company/emanate-biomedical)

## Its most-cited devices
- K083516: Periogenix (2009), cited by 1

## Recent decisions
- K083516: Periogenix (Feb 20, 2009)
- K082445: CURATIVE980 Diode Laser (Oct 15, 2008)

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