LRY
7 FDA 510(k) clearances · Product code
34 daysmedian time to decision
247 days90th percentile
7clearances measured
FDA profile
- Official device name
- Punch, Surgical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
- Adverse events (MAUDE)
- 2021: 68 · 2022: 57 · 2023: 46 · 2024: 46 · 2025: 46 · 2026: 12
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 |
|---|---|---|
| ACU-E PUNCH (K933516) | Acuderm, Inc. | 1994-03-24 |
| ELLIPSE PUNCH (K904869) | Kramer Const | 1991-03-06 |
| LIPOGEN RHEUMELISA DSDNA ASSAY (K902636) | Lipogen, Inc. | 1990-06-28 |
| BIOPSY PUNCH (K896303) | Premier Medical | 1990-02-13 |
| PIN PUNCH (K874356) | Med-Tool, Inc. | 1987-11-23 |
| TAPERED PUNCH (K874357) | Med-Tool, Inc. | 1987-11-23 |
| NAIL SET (K872388) | Med-Tool, Inc. | 1987-07-23 |
Track LRY automatically
Every clearance here is in the API, with alerts when new ones post.