FDA Registration
Active
🇺🇸 United States
GARRISON DENTAL SOLUTIONS
Reg #: 1836088
·
FEI: 3001422020
·
Expires 2026
Products
10
Proprietary Names
25
Establishment Types
4
Classifications
10
Registration Details
- Registration Name
- GARRISON DENTAL SOLUTIONS
- Registration Number
- 1836088
- FEI Number
- 3001422020
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 150 Dewitt Ln
- City
- Spring Lake
- State
- MI
- ZIP
- 49456
- Country
- US
Regulatory Submissions
- 510(k) Number
- K140144
Owner / Operator
- Firm Name
- Garrison Dental Solutions LLC
- Operator Number
- 9036522
- Address
- 150 Dewitt Lane
- City
- Spring Lake
- State
- MI
- Postal Code
- 49456
- Country
- US
- Correspondent
- David S Snellen
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Instrument, Filling, Plastic, Dental | EIY | Class 1 | Dental | No | 2006-07-31 |
| Handle, Instrument, Dental | EJB | Class 1 | Dental | No | 2014-09-02 |
| Forceps, Rubber Dam Clamp | EJG | Class 1 | Dental | No | 2013-04-10 |
| Wheel, Polishing Agent | EJQ | Class 1 | Dental | No | 2016-11-08 |
| Point, Abrasive | EHL | Class 1 | Dental | No | 2014-04-15 |
| Instruments, Dental Hand | DZN | Class 1 | Dental | No | 2019-05-30 |
| Instrument, Diamond, Dental | DZP | Class 1 | Dental | No | 2004-10-05 |
| Retainer, Matrix | JEP | Class 1 | Dental | No | 1999-02-19 |
| Disk, Abrasive | EHJ | Class 1 | Dental | No | 2016-11-08 |
| Activator, Ultraviolet, For Polymerization | EBZ | Class 2 | Dental | No | 2025-01-03 |
Proprietary Names
PerForm
Composi-Tight®
A+ Wedge
NiTin
3D Fusion
Band and Wedge Instrument
Rally
eZr
Wedge Wands®
NiTin
ClearView
3D Fusion
G Wedge
LM Instruments, Reel Matrix
FitStrip
Silver Plus
3D Clear Matrix
FenderWedge®
Varistrip Matrix
Slick Bands
Composi-Tight 3D Matrix System
Composi-Tight 3DXR Matrix System
Strata-G Sectional Matrix System
Quad Matrix System
LOOP LED Curing Light
Establishment Types
Develop Specifications But Do Not Manufacture At This Facility
Complaint File Establishment per 21 CFR 820.198
Manufacture Medical Device for Another Party (Contract Manufacturer)
Manufacture Medical Device