FDA Registration
Active
🇺🇸 United States
RANIR LLC
Reg #: 1825660
·
FEI: 1825660
·
Expires 2026
Products
14
Proprietary Names
15
Establishment Types
4
Classifications
14
Registration Details
- Registration Name
- RANIR LLC
- Registration Number
- 1825660
- FEI Number
- 1825660
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- Yes
- Address
- 4701 E PARIS AVE SE
- City
- Grand Rapids
- State
- MI
- ZIP
- 49512
- Country
- US
Regulatory Submissions
- 510(k) Number
- K091175
Owner / Operator
- Firm Name
- RANIR LLC
- Operator Number
- 1825660
- Address
- 515 Eastern Ave., --
- City
- Allegan
- State
- MI
- Postal Code
- 49010
- Country
- US
- Correspondent
- Tricia Pasek
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Mouthguard, Over-The-Counter | OBR | Class U | Unknown | No | 2009-12-01 |
| Toothbrush, Powered | JEQ | Class 1 | Dental | No | 1997-09-26 |
| Floss, Dental | JES | Class 1 | Dental | No | 1992-07-02 |
| Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile | NOB | Class 1 | Dental | No | 2021-12-07 |
| Instrument, Hand, Calculus Removal | ELA | Class 1 | Dental | No | 2017-07-05 |
| Heat Source For Bleaching Teeth | EEG | Class 1 | Dental | No | 2019-10-29 |
| Wax, Dental, Intraoral | EGD | Class 1 | Dental | No | 2011-01-06 |
| Pick, Massaging | JET | Class 1 | Dental | No | 1997-09-26 |
| Mirror, Mouth | EAX | Class 1 | Dental | No | 2009-12-01 |
| Scaler, Periodontic | EMN | Class 1 | Dental | No | 2009-12-01 |
| Toothbrush, Manual | EFW | Class 1 | Dental | No | 1992-07-02 |
| Scraper, Tongue | LCN | Class 1 | Dental | No | 2009-12-01 |
| Device, Anti-Snoring | LRK | Class 2 | Dental | No | 2010-09-13 |
| Unit, Oral Irrigation | EFS | Class 1 | Dental | No | 2021-01-18 |
Proprietary Names
Grind-No-More
POWERED TOOTHBRUSH
3G
1G
SmileSonic
Total Power
Advance Clean
EasyFlex
Polaris
Kids
Infinity
Plackers
Essential Clean USB
PLAK RX
HydroClean
Establishment Types
Complaint File Establishment per 21 CFR 820.198
Develop Specifications But Do Not Manufacture At This Facility
Repack or Relabel Medical Device
Manufacture Medical Device