Contract manufacturerLENKBAR LLC (Naples, FL)FloridaOrthopedicGeneral and plastic surgeryClass I
LENKBAR LLC
Contract manufacturer · Naples, FL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3011307621 (openFDA record; or search FDA's registration database)
- FEI number
- 3011307621
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Lenkbar LLC (FDA owner/operator no. 10048183)
- Registered address
- 2705 Corporate Flight Drive, Naples, FL 34104
- Contract listings
- 4 device listings, 4 product codes, first listed Dec 15, 2014
- 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 |
|---|---|---|---|---|---|
| HTO | Reamer | Class I | Orthopedic | Contract manufacturing | Mar 20, 2015 |
| HTW | Bit, Drill | Class I | Orthopedic | Contract manufacturing | Dec 15, 2014 |
| LXH | Orthopedic Manual Surgical Instrument | Class I | Orthopedic | Contract manufacturing | Mar 7, 2019 |
| MDM | Instrument, Manual, Surgical, General Use | Class I | General and plastic surgery | Contract manufacturing | Jul 17, 2023 |