FDA device facilities in MO

24 registered medical-device facilities with FDA recall history in MO.

• AESCULAP, INC. FEI 3003587896
• Acera Surgical - Adie Road FEI 3027386220
• BC GROUP INTERNATIONAL, INC. FEI 2939012
• BIOMERIEUX, INC. FEI 1950204
• Bausch & Lomb Incorporated FEI 1000119305
• Bausch & Lomb Incorporated FEI 1920664
• CARDINAL SCALE MFG. CO. FEI 1929045
• CERTIFIED SAFETY MFG., INC. FEI 1000158435
• Cardinal Health FEI 1921846
• GENEOSCOPY INC FEI 3026996410
• Handicare USA, Inc. FEI 3007802293
• Heritage Medical Products, inc FEI 3003881889
• JosNoe Medical Inc FEI 3000718286
• KATALYST SURGICAL, LLC FEI 3007589150
• KOVEN TECHNOLOGY, INC. FEI 1937397
• LIGHTHOUSE FOR THE BLIND FEI 1000118065
• NOA MEDICAL INDUSTRIES FEI 1000118429
• SOUTHWEST TECHNOLOGIES, INC. FEI 1929833
• STEREOTAXIS, INC. FEI 3003084417
• SYNERGETICS, INC. FEI 1000119053
• Seiler Instrument & Mfg. Co.,Inc. FEI 1927430
• Trinity Biotech (Primus Corporation dba Trinity Biotech) FEI 1931251
• Vortex Surgical FEI 3013002167
• WEXFORD LABS, INC. FEI 1000147951

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.