Benlan, Inc.
Benlan, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2014, with 1 FDA device recall on record.
Top product codes for Benlan, Inc.
FDA recalls by Benlan, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Benlan, Inc.
- K131183 — MED-RX ORAL/ENTERAL SYRINGE
- K120375 — MED-RX PATIENT DELIVERY SET
- K112799 — MED-RX EXTENSION SET WITH T-CONNECTOR
- K100700 — MED-RX PEDIATRIC FEEDING TUBES AND ACCESSORIES
- K102073 — MED-RX TRANSFER SET, MODELS 10-1227TS, 10-1300TS, 10-1305TS AND 10-1306TS
- K010607 — MED-RX IRRIGATION SET, MODEL 10-3001, 10-3002, 10-4000, 10-4001
- K990777 — MED-RX EXTENSION SETS
Data sourced from openFDA. This site is unofficial and independent of the FDA.