Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Benlan, Inc. with 7 510(k) clearances and 1 device recall. The most recent is a device recall dated Dec 11, 2015: MED-RX Single Use REF 54-3680R, 8 FR. x 36" (91CM) Polyurethane Feeding Tube For Pediatr….
| Dec 11, 2015 | MED-RX Single Use REF 54-3680R, 8 FR. x 36" (91CM) Polyurethane Feeding Tube For Pediatric Use with Orange Radiopaque Stripe and Enteral ConClass II · The product may be packaged with a 5 or 6.5FR tube instead of an 8FR size. | Device recalls |
| Jun 3, 2014 | MED-RX ORAL/ENTERAL SYRINGEK131183 · KNT | 510(k) clearances |
| Jun 28, 2012 | MED-RX PATIENT DELIVERY SETK120375 · FPA | 510(k) clearances |
| Dec 23, 2011 | MED-RX EXTENSION SET WITH T-CONNECTORK112799 · FPA | 510(k) clearances |
| Dec 13, 2010 | MED-RX PEDIATRIC FEEDING TUBES AND ACCESSORIESK100700 · FPD | 510(k) clearances |
| Nov 8, 2010 | MED-RX TRANSFER SET, MODELS 10-1227TS, 10-1300TS, 10-1305TS AND 10-1306TSK102073 · FPA | 510(k) clearances |
| Nov 28, 2001 | MED-RX IRRIGATION SET, MODEL 10-3001, 10-3002, 10-4000, 10-4001K010607 · LJH | 510(k) clearances |
| Aug 25, 1999 | MED-RX EXTENSION SETSK990777 · FPA | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
