# Limbus Ai, Inc.

- Location (FDA's records): Regina, CA
- FDA decisions: 3 (2020–2024): 3 510(k) clearances
- Product codes: LLZ (2), QKB (1)
- 510(k) review time since 2016: median 98 days, against 157 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 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
- Microsoft Corp.: 1 (https://510kreport.com/company/microsoft)

## Its most-cited devices
- K201232: Limbus Contour (2020), cited by 1
- K230575: Limbus Contour (2023), cited by 1

## Recent decisions
- K241837: Limbus Contour (Oct 9, 2024)
- K230575: Limbus Contour (Apr 7, 2023)
- K201232: Limbus Contour (Aug 13, 2020)

Source page: https://510kreport.com/company/limbus-ai