Hologic, Inc.
Hologic, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2026, with 48 FDA device recalls on record.
Clearances by Hologic, Inc. — page 2
101–118 of 118- K992677 — EAGLE OPTION FOR THE QDR BONE DENSITOMETER, MODELS QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W
- K983028 — FRACTURE RISK OPTION FOR THE QDR BONE DENSITOMETER, MODEL#S QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W
- K974058 — FS IV MINI C-ARM SYSTEM
- K961787 — BODY COMPOSITION SOFTWARE OPTION FOR QDR X-RAY BONE DENSITOMETERS
- K963363 — HOLOGIC QDR SERIES X-RAY BOE DENSITOMETERS
- K941362 — BONE MINERAL DENSITOMETER
- K943505 — HOLOGIC QDR-3000 X-RAY BONE DENSITOMETER
- K926300 — DTX-100
- K913321 — HOLOGIC QDR-2000 X-RAY BONE DENSITOMETER
- K913757 — HOLOGIC CER 20/20, COMPUTED EQUAL RADIO DIAG CHEST
- K905753 — QDR-1000 AND QDR-1000/W X-RAY BONE DENSITOMETER
- K905691 — QDR-1000 AND WITH X-RAY BONE DENSITOMETER
- K894795 — HOLOGIC QDR-1000/W X-RAY BONE DENSITOMETER
- K890999 — MODIFIED QDR-1000 X-RAY BONE DENSITOMETER
- K883280 — HOLOGIC QDR-1000 X-RAY BONE DENSITOMETER/MODIFIED
- K883360 — HOLOGIC MODEL WHF-1 ANTHROPOMORPHIC FEMUR PHANTOM
- K871446 — HOLOGIC MODELS BLK-1, DPA/QDR-1 & QCT-1
- K871553 — X-CALIBER MODEL 1000 BONE MINERAL ANALYZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.