CCX
8 FDA 510(k) clearances · Product code
32 daysmedian time to decision
146 days90th percentile
8clearances measured
FDA profile
- Official device name
- Support, Patient Position
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.6820
- Medical specialty
- Anesthesiology
- Adverse events (MAUDE)
- 2020: 13 · 2021: 26 · 2022: 13 · 2024: 23 · 2025: 22 · 2026: 27
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CHIN UP (K943837) | Edward Carden | 1994-10-14 |
| VILA-COOKE(TM) ANESTHESIA PILLOW (K932305) | Sharn, Inc. | 1993-10-05 |
| SNIFF POSITION PILLOW (K934235) | American Medical Development, Inc. | 1993-10-01 |
| SURGICAL HEAD SUPPORT (K861915) | Treace Medical, Inc. | 1986-05-30 |
| AIR UTERINE DISPLACER-AUD 120 (K833022) | Scientific Sales Intl., Inc. | 1983-10-14 |
| VARI-SUPPORT LOW BACK POSTURE PILLOW (K821838) | Body Therapeutics, Inc. | 1982-07-20 |
| PRENATAL SUPPORT PILLOW (K810035) | Supportech, Inc. | 1981-01-23 |
| ANSPACH LEG SUPPORT (K801330) | The Anspach Effort, Inc. | 1980-06-26 |
Track CCX automatically
Every clearance here is in the API, with alerts when new ones post.