IontoPatch
GUDID 10815611020005
The IontoPatch contains an innovative self-contained battery that produces an electric current to carry drug molecules non-invasively across the skin and to underlying tissue. There is no need for an external power source. Drug delivery is shut off automatically when the prescribed dosage has been administered. The IontoPatch is single use and disposable. Since there are no external batteries or wires, patients are able to return to their daily activities wearing the patch and receiving time-released iontophoresis.
TAPEMARK COMPANY, THE
Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch Drug-delivery iontophoresis patch| Primary Device ID | 10815611020005 |
| NIH Device Record Key | 44846405-e60a-4500-9480-36a613a41346 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IontoPatch |
| Version Model Number | STAT |
| Company DUNS | 006154595 |
| Company Name | TAPEMARK COMPANY, THE |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com | |
| Phone | 612-245-7088 |
| mezzettj@tapemark.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10815611020005 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K992708
FDA Product Code
| EGJ | Device, Iontophoresis, Other Uses |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-10-30 |
| Device Publish Date | 2016-10-03 |
On-Brand Devices [IontoPatch]
| 10815611020036 | The IontoPatch contains an innovative self-contained battery that produces an electric current t |
| 10815611020029 | The IontoPatch contains an innovative self-contained battery that produces an electric current t |
| 10815611020012 | The IontoPatch contains an innovative self-contained battery that produces an electric current t |
| 10815611020005 | The IontoPatch contains an innovative self-contained battery that produces an electric current t |
Trademark Results [IontoPatch]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 IONTOPATCH 90904223 not registered Live/Pending |
The Tapemark Company 2021-08-26 |
 IONTOPATCH 88879607 not registered Live/Pending |
The Tapemark Company 2020-04-20 |
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