# Medicel AG

- Location (FDA's records): Hasbrouck Heights, NJ
- FDA decisions: 7 (1999–2025): 7 510(k) clearances
- Names in FDA's records: Medicel AG (6); Medicel, S.A. DE C.V. (1)
- Product codes: MSS (5), KYB (1), KCT (1)
- Predicates its devices cite: 7 (4 its own); citations of its devices by later devices: 9 (4 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Allergan, Inc.: 1 (https://510kreport.com/company/allergan)
- Alcon Research, Ltd.: 1 (https://510kreport.com/company/alcon-research)
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)

## Firms that cite its devices most
- Lenstec, Inc.: 2 (https://510kreport.com/company/lenstec)
- Asico, LLC: 2 (https://510kreport.com/company/asico)
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)

## Its most-cited devices
- K040837: Multiject Injector and Microglide Cartridge (2004), cited by 4
- K092023: Naviject SUB2-1P, Model: LP604430 (2009), cited by 3
- K101134: Visian Nanopoint 2.0 Injector Model LP604430 (2010), cited by 1
- K070669: Iol Injector Set (2007), cited by 1

## Recent decisions
- K252540: ACCUJECT Injector Set 2.1-1P (LP604590) (Sep 16, 2025)
- K231106: Accuject Refra Injector AR2900 (Sep 19, 2023)
- K101134: Visian Nanopoint 2.0 Injector Model LP604430 (Aug 9, 2010)
- K092023: Naviject SUB2-1P, Model: LP604430 (Jul 28, 2009)
- K070669: Iol Injector Set (Nov 1, 2007)
- K040837: Multiject Injector and Microglide Cartridge (Jun 17, 2004)
- K972719: Claricel Sterilization Pouches and Sterilization Reels (Feb 4, 1999)

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