Is this your brand? Sign in to claim ownership.
Sign in to claim this brandGeneral Medical Co.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 5011 Gate Parkway, Bldg. 100, Jacksonville, FL, 32256
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3013399500
- DUNS Number
- —
Catalogue (31)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Drionic TM | Hand-Foot Pads | FDA UDI | Class II | Active |
| Drionic TM | Underarm Sweat Stop | FDA UDI | Class II | Active |
| Drionic TM | Underarm Parts Kit | FDA UDI | Class II | Active |
| Drionic TM | Hand/Foot Sweat Stop | FDA UDI | Class II | Active |
| Drionic TM | Hand/Foot Parts Kit | FDA UDI | Class II | Active |
| Drionic TM | Pair Underarm Devices | FDA UDI | Class II | Active |
| Drionic TM | LG Alkaline Battery | FDA UDI | Class II | Active |
| Drionic TM | Hand-Foot Plates | FDA UDI | Class II | Active |
| Drionic TM | Hand/Foot Large Parts Kit | FDA UDI | Class II | Active |
| Drionic TM | Pair LG Alkaline Batteries | FDA UDI | Class II | Active |
| Drionic TM | Pair Hand/Foot Devices | FDA UDI | Class II | Active |
| Drionic TM | Underarm Pads | FDA UDI | Class II | Active |
| Drionic TM | Underarm Straps | FDA UDI | Class II | Active |
| Drionic TM | Underarm Modules | FDA UDI | Class II | Active |
| Drionic TM | Underarm Large Parts Kit | FDA UDI | Class II | Active |
| Pd-Pak | K933619 | FDA 510(k) | Class II | Active |
| Air Viva Ii | K802231 | FDA 510(k) | Class II | Active |
| Exam Gown | K770476 | FDA 510(k) | Class I | Active |
| Sterilization Wrap | K820521 | FDA 510(k) | Class II | Active |
| Medi-Pak Lemon Glyceoin Swabs | K770583 | FDA 510(k) | Class I | Active |
| Operand Lubricating Jelly | K912975 | FDA 510(k) | Class I | Active |
| C.s.r. Wrappers | K820689 | FDA 510(k) | Class II | Active |
| Operand* Lubricating Jelly | K900110 | FDA 510(k) | Class I | Active |
| Drionic | K831320 | FDA 510(k) | Class II | Active |
| Procedure Kit | K926269 | FDA 510(k) | Class II | Active |
| Genesis Insufflating Catheter | K903669 | FDA 510(k) | Class I | Active |
| C.a.s.e. Container | K844652 | FDA 510(k) | Class I | Active |
| Operand Lubricating Jelly | K912132 | FDA 510(k) | Class II | Active |
| Subderm Tm | K853635 | FDA 510(k) | Class II | Active |
| Isolation Gown | K770488 | FDA 510(k) | Class II | Active |
| Laparotomy Spogne | K772089 | FDA 510(k) | U | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.