JOK
7 FDA 510(k) clearances · Product code
56 daysmedian time to decision
84 days90th percentile
7clearances measured
FDA profile
- Official device name
- Scissors, Medical, Disposable
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6820
- Medical specialty
- General Hospital
- Adverse events (MAUDE)
- 1994: 1 · 1995: 1 · 2002: 4
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 |
|---|---|---|
| SUTURE REMOVAL KIT (K855131) | Dynarex Corp. | 1986-01-13 |
| UTILITY SCISSORS DISPOSABLE ITEMS (K843075) | Greene International Corp. | 1984-09-05 |
| DISPOSABLE SUTURE REMOVAL SCISSORS (K812555) | Medcare Products | 1981-11-16 |
| SUTURE REMOVAL SET (K770595) | Abco Dealers, Inc. | 1977-05-23 |
| SHEAR, PLASTIC HANDLE UTILITY S-475-7 (K770481) | Acme United Corp. | 1977-04-29 |
| SUTURE CUTTER (K770163) | Concept, Inc. | 1977-03-30 |
| DRESSING CHANGE KIT (K761192) | Superior Plastic Products Corp. | 1977-02-28 |
Track JOK automatically
Every clearance here is in the API, with alerts when new ones post.