Data / Medical devices / United States / Tesla Biohealing, Inc.
Tesla Biohealing, Inc.: FDA-registered device maker in Milford, DE, United States, 1 510(k) clearance
Tesla Biohealing, Inc. is registered with the FDA (registration 3023229437) in Milford, DE, United States. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 22, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023229437
- Address
- 111 Mccoy St, Milford, DE, United States, 19963
- Owner or operator
- Tesla BioHealing, Inc. (10085605)
- Roles
- Contract manufacturer, Manufacturer, Remanufacturer, Specification developer
- First device listed
- July 8, 2022
- Registered through
- 2026
- Brand names listed
- FemaCare, ForceBeyond, NasalCare®, Tesla BioHealing, Tesla BioHealing®
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bed, Manual | FNJ | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Blower, Powder, Ent | KCL | 1 | Manufacturer | accessdata.fda.gov |
| Douche Apparatus, Vaginal, Therapeutic | HED | 1 | Manufacturer | accessdata.fda.gov |
| Foot Wrap For Treating Restless Leg Syndrome Symptoms | OTX | 1 | Manufacturer | accessdata.fda.gov |
| Irrigator, Powered Nasal | KMA | 1 | Manufacturer | accessdata.fda.gov |
| Joint, Ankle, External Brace | ITW | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Contract manufacturer, Manufacturer, Remanufacturer | accessdata.fda.gov |
| Nasal Spray, Ent Delivery | KCO | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Nebulizer, Manual | EPN | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 22, 2003 | K030056 | WORRY-REMOVER IRRIGATOR | HED | Substantially Equivalent | Corisen Group, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Blower, Powder, Ent
- All makers of Douche Apparatus, Vaginal, Therapeutic
- All makers of Foot Wrap For Treating Restless Leg Syndrome Symptoms
- All makers of Joint, Ankle, External Brace
- All makers of Pump, Nebulizer, Manual
- All makers of Bed, Manual
Updated April 22, 2003. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.