# A & E Medical Corporation

- Location (FDA's records): Farmingdale, NJ
- FDA decisions: 4 (2018–2020): 4 510(k) clearances
- Product codes: JDQ (4)
- 510(k) review time since 2016: median 93 days, against 101 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.): 2 (https://510kreport.com/company/pioneer-surgical-technology-dba-rti-surgical)
- Biomet Microfixation: 2 (https://510kreport.com/company/biomet-microfixation)
- Pioneer Surgical Technology: 1 (https://510kreport.com/company/pioneer-surgical-technology)
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)

## Its most-cited devices
- K180582: Sternal Cable System (2018), cited by 1
- K173579: Thorecon™ Fixation System (2018), cited by 1

## Recent decisions
- K193479: Sternal Cable System (Mar 23, 2020)
- K181607: Thorecon Rigid Fixation System (Oct 12, 2018)
- K180582: Sternal Cable System (May 31, 2018)
- K173579: Thorecon™ Fixation System (Feb 12, 2018)

Source page: https://510kreport.com/company/a-e-medical