FDA device facilities in MD

17 registered medical-device facilities with FDA recall history in MD.

• ACELL, INC. FEI 3005920706
• Accora Inc FEI 3013254491
• Alcon Vision, LLC FEI 3000215259
• BECTON, DICKINSON & CO. FEI 1119779
• BECTON, DICKINSON & CO. FEI 1111096
• BTE TECHNOLOGIES FEI 1119903
• Breethe, Inc. FEI 3014990448
• CORBIN CLINICAL RESOURCES, LLC FEI 3012975098
• Life Technologies Corporation FEI 3003335080
• Longhorn Vaccines and Diagnostics LLC FEI 3011818318
• QIAGEN FEI 3003572099
• Senseonics, Inc. FEI 3009862700
• TERUMO CARDIOVASCULAR SYSTEMS CORPORATION FEI 3000204839
• TERUMO MEDICAL CORP. FEI 1118880
• TRINITY STERILE, INC. FEI 1000123297
• W. L. GORE & ASSOCIATES, INC. FEI 3003910212
• XCISION MEDICAL SYSTEMS, LLC FEI 3014273653

Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. We restate the public record only — measured facts, never risk verdicts.