# Medeon Biodesign, Inc.

- Location (FDA's records): Taipei, TW
- FDA decisions: 7 (2015–2020): 7 510(k) clearances
- Product codes: GCJ (5), OCW (2)
- 510(k) review time since 2016: median 32 days, against 69 for FDA's reviews in the same codes and years (4 of 4 faster)
- Predicates its devices cite: 7 (5 its own); citations of its devices by later devices: 7 (5 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
- Teleflexmedical, Inc.: 1 (https://510kreport.com/company/teleflexmedical)
- Minimally Invasive Devices, LLC: 1 (https://510kreport.com/company/minimally-invasive-devices)

## Firms that cite its devices most
- TroCare, LLC: 1 (https://510kreport.com/company/trocare)
- Clearcam, LLC: 1 (https://510kreport.com/company/clearcam)

## Its most-cited devices
- K192891: Laparoscope Lens Shield Device (LENS) (2019), cited by 2
- K170103: Laparoscope Lens Shield Device (LENS) (2017), cited by 2
- K160117: AbClose - Port Site Closure Device (2016), cited by 1
- K151117: Laparoscope Lens Shield Device (2015), cited by 1
- K160172: Laparoscope Lens Shield Device (2016), cited by 1

## Recent decisions
- K200902: ClickClean (Apr 30, 2020)
- K193652: AbClose - Port Site Closure Device (Mar 26, 2020)
- K192891: Laparoscope Lens Shield Device (LENS) (Nov 7, 2019)
- K170103: Laparoscope Lens Shield Device (LENS) (Feb 16, 2017)
- K160117: AbClose - Port Site Closure Device (Sep 9, 2016)
- K160172: Laparoscope Lens Shield Device (Apr 21, 2016)
- K151117: Laparoscope Lens Shield Device (Aug 20, 2015)

Source page: https://510kreport.com/company/medeon-biodesign