# Oxis Intl., Inc.

- Location (FDA's records): Portland, OR
- FDA decisions: 11 (1995–1997): 11 510(k) clearances
- Product codes: LGQ (2), LGR (1), LAS (1), DLJ (1), KLQ (1), JTO (1), LGS (1), MSL (1), LBZ (1), LCQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Seradyn, Inc.: 2 (https://510kreport.com/company/seradyn)
- Ark Diagnostics, Inc.: 2 (https://510kreport.com/company/ark-diagnostics)

## Its most-cited devices
- K955562: Innofluor Phenytoin Assay System (1996), cited by 1
- K970517: Innofluor Topiramate Control Set (1997), cited by 1
- K970509: Innoflour Calibrator Reagent Set (1997), cited by 1
- K970510: Innoflour Topiramate Reagent Set (1997), cited by 1

## Recent decisions
- K972331: Innofluor Gentamicin Assay System (Aug 1, 1997)
- K972330: Innofluor Phenobarbital Assay System (Jul 14, 1997)
- K970517: Innofluor Topiramate Control Set (May 12, 1997)
- K970509: Innoflour Calibrator Reagent Set (May 12, 1997)
- K970510: Innoflour Topiramate Reagent Set (May 12, 1997)
- K955568: Innofluor Quinidine Assay System (Apr 4, 1996)
- K955570: Innofluor Amikacin Assay System (Feb 9, 1996)
- K955569: Innofluor Gentamicin Assay System (Feb 9, 1996)

Source page: https://510kreport.com/company/oxis-intl