Contract manufacturerContract sterilizerLaunchPort LLC (Baltimore, MD)MarylandEar, nose and throatNeurologyGastroenterology and urologyClass IClass II
LaunchPort LLC
Contract manufacturer and sterilizer · Baltimore, MD
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3015259858 (openFDA record; or search FDA's registration database)
- FEI number
- 3015259858
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer; Contract sterilizer
- Owner or operator
- LaunchPort LLC (FDA owner/operator no. 10083736)
- Registered address
- 101 West Dickman St. Suite 900, Baltimore, MD 21230
- Contract listings
- 5 device listings, 6 product codes, first listed Dec 15, 2021
- 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 |
|---|---|---|---|---|---|
| ESE | Larynx, Artificial (Battery-Powered) | Class I | Ear, nose and throat | Contract manufacturing | Dec 15, 2021 |
| GXN | Plate, Cranioplasty, Preformed, Non-Alterable | Class II | Neurology | Contract sterilization | Dec 15, 2021 |
| KGC | Tube, Gastro-Enterostomy | Class II | Gastroenterology and urology | Contract manufacturing | Apr 18, 2024 |
| KTH | Device, Anti-Stammering | Class I | Ear, nose and throat | Contract manufacturing | Dec 15, 2021 |
| OKP | Transcranial Magnetic Stimulator For The Treatment Of Migraine Headache | Class II | Neurology | Contract manufacturing | Dec 15, 2021 |
| PJN | Filler, Bone Void, Non-Alterable Compound For Cranioplasty | Class II | Neurology | Contract sterilization | Dec 15, 2021 |