KOQ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.3410
- Medical specialty
- Dental
- Adverse events (MAUDE)
- 2002: 2
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 |
|---|---|---|
| URESIL ENDOSCOPIC LASER OVERTUBE (K901882) | Uresil Corp. | 1990-07-27 |
| NAS&P GRASPING FORCEPS & ASSOC. DEVICES (K900401) | North American Sterilization & Packaging Co. | 1990-02-09 |
| OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE (K896821) | North American Sterilization & Packaging Co. | 1990-02-09 |
| DENTOLOCK DENTURE ADHESIVE CREAM (K831265) | Solar Dental Co., Inc. | 1983-05-09 |
Track KOQ automatically
Every clearance here is in the API, with alerts when new ones post.