# Aspire Bariatrics, Inc.

- Location (FDA's records): King Of Prussia, PA
- FDA decisions: 3 (2016–2018): 2 510(k) clearances and 1 original PMA approval
- Product codes: KNT (2), OYF (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (0 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
- Specialized Health Products International, Inc.: 1 (https://510kreport.com/company/specialized-health-products-international)
- Teleflex Medical: 1 (https://510kreport.com/company/teleflex-medical)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Conmedcorp: 1 (https://510kreport.com/company/conmedcorp)

## Recent decisions
- K182248: Aspire Venting Tube (Nov 13, 2018)
- K180725: Aspire Introducer Needle (Jul 11, 2018)
- P150024: AspireAssist (Jun 14, 2016)

Source page: https://510kreport.com/company/aspire-bariatrics