Data / Medical devices / United States / JB Medical Development, LLC Dba/Md3, LLC
JB Medical Development, LLC Dba/Md3, LLC: FDA-registered device maker in Sunrise, FL, United States, 1 510(k) clearance
JB Medical Development, LLC Dba/Md3, LLC is registered with the FDA (registration 3011749806) in Sunrise, FL, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 7, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011749806
- Address
- 4534 N Hiatus Road, Sunrise, FL, United States, 33351
- Owner or operator
- JB Medical Development, LLC dba/MD3, LLC (10055465)
- Roles
- Complaint file establishment, Repackager or relabeler, Specification developer
- First device listed
- July 27, 2017
- Registered through
- 2026
- Brand names listed
- BIO-SAV, ORDOCK 2 CUPS, DISPOSABLE, ORDOCK PLATFORM, REUSABLE, PREFERX DELIVERY SYSTEM, DISPOSABLE, aParent Carpal Tunnel Disposable Surgical Kit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bone Mill | LYS | 1 | Specification developer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Specification developer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Specification developer | accessdata.fda.gov |
| Tray, Surgical | LRP | 1 | Specification developer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Complaint file establishment, Repackager or relabeler, Specification developer | 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 |
|---|---|---|---|---|---|---|
| September 7, 2021 | K210997 | PreferX Delivery System | FMF | Substantially Equivalent | Md3, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Bone Mill
- All makers of Tray, Surgical, Instrument
- All makers of Tray, Surgical
- All makers of Orthopedic Manual Surgical Instrument
Updated September 7, 2021. 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.