Contract manufacturerDEMETECH CORP. (Miami Lakes, FL)FloridaObstetrics and gynecologyHematologyClass IIClass I
DEMETECH CORP.
Contract manufacturer ยท Miami Lakes, FL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1064584 (openFDA record; or search FDA's registration database)
- FEI number
- 3003063934
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Manufacturer; Contract manufacturer
- Owner or operator
- DEMETECH CORP. (FDA owner/operator no. 9041973)
- Registered address
- 5980 Miami Lakes Drive, Miami Lakes, FL 33014
- Contract listings
- 2 device listings, 2 product codes, first listed Feb 1, 2023
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| HIF | Insufflator, Laparoscopic | Class II | Obstetrics and gynecology | Contract manufacturing | Feb 1, 2023 |
| KST | System, Blood Collection, Vacuum-Assisted, Manual | Class I | Hematology | Contract manufacturing | Nov 14, 2023 |