# Aeiomed, Inc.

- Location (FDA's records): Stoughton, WI
- FDA decisions: 4 (2004–2010): 4 510(k) clearances
- Product codes: BZD (4)
- Predicates its devices cite: 9 (3 its own); citations of its devices by later devices: 8 (3 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
- Respironics, Inc.: 2 (https://510kreport.com/company/respironics)
- Vital Signs, Inc.: 1 (https://510kreport.com/company/vital-signs)
- Resmed, Ltd.: 1 (https://510kreport.com/company/resmed)
- Hoffman Laboratories, LLC: 1 (https://510kreport.com/company/hoffman-laboratories)
- Innomed Technologies: 1 (https://510kreport.com/company/innomed-technologies)

## Firms that cite its devices most
- Somnetics International, Inc.: 1 (https://510kreport.com/company/somnetics-international)
- Deshum Medical: 1 (https://510kreport.com/company/deshum-medical)
- Innomed Technologies, Inc./Respcare, Inc.: 1 (https://510kreport.com/company/innomed-technologies-respcare)
- Insleep Technologies, LLC: 1 (https://510kreport.com/company/insleep-technologies)
- Human Design Medical, LLC: 1 (https://510kreport.com/company/human-design-medical)

## Its most-cited devices
- K100121: Model 300157 Cpap System (2010), cited by 4
- K042130: Aura Cpap Patient Interface (2004), cited by 2
- K042945: Aura Cpap System (2005), cited by 1
- K072993: Reusable Headrest with Nasal Seal (2008), cited by 1

## Recent decisions
- K100121: Model 300157 Cpap System (Jul 13, 2010)
- K072993: Reusable Headrest with Nasal Seal (Feb 8, 2008)
- K042945: Aura Cpap System (Mar 9, 2005)
- K042130: Aura Cpap Patient Interface (Sep 8, 2004)

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