HRR
8 FDA 510(k) clearances · Product code
37 daysmedian time to decision
63 days90th percentile
8clearances measured
FDA profile
- Official device name
- Scissors, Orthopedic, Surgical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.4540
- Medical specialty
- Orthopedic
- Adverse events (MAUDE)
- 1994: 1 · 1996: 1 · 1997: 1 · 1998: 1 · 1999: 2 · 2000: 3
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 |
|---|---|---|
| MICROSURGICAL SCISSORS (K890212) | Kinetic Medical Products | 1989-01-27 |
| SURGICAL SCISSORS (K890225) | Kinetic Medical Products | 1989-01-27 |
| TRIGEMINAL SCISSORS (K890261) | Kinetic Medical Products | 1989-01-27 |
| SCISSOR, LEFT (K873501) | Arthropedics, Inc. | 1987-11-02 |
| SCISSOR, RIGHT (K873502) | Arthropedics, Inc. | 1987-11-02 |
| 69-100 TO 69-114 VARIOUS CUTICLE SCISSORS (K851800) | Artiberia | 1985-06-20 |
| ALL-HANDS MEDICAL SUPPLY SUTURE REMOVAL (K842953) | All-Hands Medical Supply, Inc. | 1984-08-21 |
| GENERAL UTILITY SURG. SCISSORS #460180- (K800721) | Edward Weck, Inc. | 1980-05-08 |
Track HRR automatically
Every clearance here is in the API, with alerts when new ones post.