# Rebound Therapeutics

- Location (FDA's records): Irvine, CA
- FDA decisions: 8 (2018–2023): 8 510(k) clearances
- Names in FDA's records: Rebound Therapeutics (6); Rebound Therapeutics Corporation (2)
- Product codes: GEI (4), GWG (4)
- 510(k) review time since 2016: median 59 days, against 146 for FDA's reviews in the same codes and years (5 of 7 faster)
- Predicates its devices cite: 10 (5 its own); citations of its devices by later devices: 7 (5 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Nico Corporation: 2 (https://510kreport.com/company/nico)
- Kirwan Surgical Products, Inc.: 2 (https://510kreport.com/company/kirwan-surgical-products)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)

## Firms that cite its devices most
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)
- Clearmind Biomedical: 1 (https://510kreport.com/company/clearmind-biomedical)

## Its most-cited devices
- K201840: Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box) (2020), cited by 2
- K182211: Aurora Surgiscope System (2019), cited by 1
- K201637: Aurora Evacuator +Coag (2020), cited by 1
- K203745: AURORA Evacuator +Coag (2021), cited by 1
- K180372: Aurora Evacuator (2018), cited by 1
- K191861: Aurora Surgiscope System (2019), cited by 1

## Recent decisions
- K232618: Aurora Surgiscope System (Oct 27, 2023)
- K203745: AURORA Evacuator +Coag (Dec 2, 2021)
- K201840: Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box) (Nov 4, 2020)
- K201637: Aurora Evacuator +Coag (Aug 12, 2020)
- K191861: Aurora Surgiscope System (Dec 6, 2019)
- K190075: Aurora Evacuator (Feb 12, 2019)
- K182211: Aurora Surgiscope System (Jan 18, 2019)
- K180372: Aurora Evacuator (Apr 9, 2018)

Source page: https://510kreport.com/company/rebound-therapeutics