# Bpendo, LLC

- Location (FDA's records): Norman, OK
- FDA decisions: 2 (2022–2026): 2 510(k) clearances
- Names in FDA's records: Bpendo, LLC (1); BPEndo, LLC (1)
- Product codes: FDF (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Lumendi, LLC: 1 (https://510kreport.com/company/lumendi)

## Its most-cited devices
- K213773: Insufflation Retention Device (2022), cited by 1

## Recent decisions
- K261587: Insufflation Retention Device (IRD) (11173-325-101) (Jul 2, 2026)
- K213773: Insufflation Retention Device (Jul 21, 2022)

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