State
FDA device facilities in MI
30 registered medical-device facilities with FDA recall history in MI.
- ASPEN SURGICAL PRODUCTS, INC. FEI 3002750084
- AmFab Co., LLC FEI 1831748
- BIOPRO, INC. FEI 1832656
- HORIBA INSTRUMENTS INCORPORATED FEI 1827821
- HUDSON SCIENTIFIC LLC FEI 3013037032
- MAR-MED Inc. FEI 1832653
- MC3, Inc. FEI 3011468686
- MED MICHIGAN HOLDINGS LLC FEI 3017540705
- METREX RESEARCH FEI 1000117344
- MICHIGAN INSTRUMENTS FEI 1821850
- Materialise USA, LLC. FEI 3005718816
- Medtronic Grand Rapids FEI 3003955307
- Oxus America, Inc. FEI 3008841036
- PHADIA US INC. FEI 3004973408
- PHARMACIA & UPJOHN COMPANY LLC FEI 1810189
- Pioneer Surgical Technology, Inc. FEI 1000115331
- RANIR LLC FEI 1825660
- ROCKWELL MEDICAL FEI 3001236991
- SAFE N SIMPLE LLC FEI 3008374791
- SIEMENS MEDICAL SOLUTIONS USA, INC. FEI 3003304172
- STRYKER CORP. FEI 1811755
- STRYKER MANUFACTURING KALAMAZOO FEI 3007997036
- STRYKER MEDICAL FEI 1831750
- Skytron, LLC FEI 1825014
- Stryker Instruments FEI 3015967359
- SunMed Group Holdings, LLC FEI 1314417
- TECH GROUP GRAND RAPIDS, INC. FEI 3003595336
- THE STANDING COMPANY FEI 3007494904
- Xoran Technologies, LLC FEI 3004198450
- Zimmer U.S., Inc. Connected Health FEI 3020393263
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.