FDA Registration
Active
🇺🇸 United States
DYNAMIC DIAGNOSTICS INCORPORATED
Reg #: 3010230734
·
FEI: 3010230734
·
Expires 2026
Products
10
Proprietary Names
3
Establishment Types
3
Classifications
10
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Registration Details
- Registration Name
- DYNAMIC DIAGNOSTICS INCORPORATED
- Registration Number
- 3010230734
- FEI Number
- 3010230734
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- Yes
- Address
- 800 Junction St
- City
- Plymouth
- State
- MI
- ZIP
- 48170
- Country
- US
Regulatory Submissions
- 510(k) Number
- K073360
Owner / Operator
- Firm Name
- Dynamic Diagnostics Incorporated
- Operator Number
- 10044579
- Address
- 800 Junction St
- City
- Plymouth
- State
- MI
- Postal Code
- 48170
- Country
- US
- Correspondent
- Trevor Tynan
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | Class 2 | General, Plastic Surgery | No | 2019-03-13 |
| Endoscopic Irrigation/Suction System | OCX | Class 2 | Gastroenterology, Urology | No | 2025-02-19 |
| Tray, Biopsy, Without Biopsy Instruments | FCH | Class 1 | Gastroenterology, Urology | No | 2019-03-13 |
| Accessories, Cleaning Brushes, For Endoscope | MNL | Class 1 | Gastroenterology, Urology | No | 2022-03-09 |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | Class 1 | Ophthalmic | No | 2025-02-27 |
| Endoscopic Bite Block | MNK | Class 1 | Gastroenterology, Urology | No | 2019-03-12 |
| Endoscope Channel Accessory | ODC | Class 2 | Gastroenterology, Urology | No | 2025-02-19 |
| Kit, Screening, Urine | JXA | Class 1 | Microbiology | No | 2019-03-13 |
| Electrosurgical Patient Return Electrode | ODR | Class 2 | General, Plastic Surgery | No | 2019-03-13 |
| Apparatus, Exhaust, Surgical | FYD | Class 2 | General, Plastic Surgery | No | 2025-02-19 |
Proprietary Names
Endoscopy Kit
Post Op Eye Kit
Urinalysis Kit
Establishment Types
Repack or Relabel Medical Device
Manufacture Medical Device
Develop Specifications But Do Not Manufacture At This Facility