# General Project S.R.L.

- Location (FDA's records): North Reading, MA
- FDA decisions: 6 (2001–2016): 6 510(k) clearances
- Names in FDA's records: General Project S.R.L. (5); General Project (1)
- Product codes: GEX (3), IMI (3)
- Predicates its devices cite: 17 (3 its own); citations of its devices by later devices: 5 (3 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
- Emed, Inc.: 2 (https://510kreport.com/company/emed)
- Sybaritic, Inc.: 2 (https://510kreport.com/company/sybaritic)
- Palomar Medical Products, Inc.: 2 (https://510kreport.com/company/palomar-medical-products)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)
- Physio Technology, Inc.: 1 (https://510kreport.com/company/physio-technology)
- Palomar Medical Technologies, Inc.: 1 (https://510kreport.com/company/palomar-medical-technologies)
- Palomar: 1 (https://510kreport.com/company/palomar)
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)

## Firms that cite its devices most
- Radiancy (Israel), Ltd.: 1 (https://510kreport.com/company/radiancy-israel)
- Alma Lasers, Inc.: 1 (https://510kreport.com/company/alma-lasers)

## Its most-cited devices
- K091615: Med Contour (2010), cited by 2
- K051508: Med Flash II Intense Pulsed Light System. (2005), cited by 2
- K053041: Med Sculpt (2006), cited by 1

## Recent decisions
- K161502: MC1 Plus (Aug 16, 2016)
- K091615: Med Contour (May 6, 2010)
- K062312: Axiom Pulsed Light System (Oct 16, 2006)
- K053041: Med Sculpt (Aug 2, 2006)
- K051508: Med Flash II Intense Pulsed Light System. (Oct 5, 2005)
- K004014: MD 30 Compact (Mar 16, 2001)

Source page: https://510kreport.com/company/general-project