# Energist, Ltd.

- Location (FDA's records): Swansea, GB
- FDA decisions: 4 (2006–2023): 4 510(k) clearances
- Names in FDA's records: Energist, Ltd. (3); Energist Limited (1)
- Product codes: GEX (2), GEI (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (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
- Rhytec Incorporated: 2 (https://510kreport.com/company/rhytec)
- Mccue Plc: 1 (https://510kreport.com/company/mccue)
- Cyden Limited: 1 (https://510kreport.com/company/cyden)

## Firms that cite its devices most
- Apyx Medical Corporation (Formerly Bovie Medical Corporation): 1 (https://510kreport.com/company/apyx-medical-formerly-bovie-medical)

## Its most-cited devices
- K132754: Neogen PSR System (2013), cited by 2

## Recent decisions
- K221873: NeoGen PSR System (Jan 12, 2023)
- K132754: Neogen PSR System (Dec 12, 2013)
- K082825: Energist Ultraplus Variable Pulsed Light (VPL) System (Feb 6, 2009)
- K060216: Energist Ultra VPL Intense Pulse Light System (Mar 16, 2006)

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