Data / Medical devices / United States / Hartman Medical Group,LLC
Hartman Medical Group,LLC: FDA-registered device maker in Birmingham, AL, United States, 5 510(k) clearances
Hartman Medical Group,LLC is registered with the FDA (registration 3017567825) in Birmingham, AL, United States. It lists 6 device types. The FDA files 5 510(k) clearances under its listings, the newest dated July 6, 2026. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3017567825
- Address
- 2700 Corporate Drive Suite 200, Birmingham, AL, United States, 35242
- Owner or operator
- Hartman Medical Group (10078696)
- Roles
- Complaint file establishment, Repackager or relabeler, Specification developer
- First device listed
- November 2, 2020
- Registered through
- 2026
- Brand names listed
- HMG, HMG Blood Transfer Device, HMG Facial Cannula, HMG IV admin Pump sets, HMG Needleless PRN connector, HMG Spinal Needle, Infiltration Tubing, Introducer Kit and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Complaint file establishment | accessdata.fda.gov |
| Introducer, Catheter | DYB | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Needle, Conduction, Anesthetic (W/Wo Introducer) | BSP | 2 | Complaint file establishment | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| System, Blood Collection, Vacuum-Assisted, Manual | KST | 1 | Complaint file establishment | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| July 6, 2026 | K261529 | Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04) | DYB | Substantially Equivalent | Hartman Medical Group, LLC | accessdata.fda.gov |
| April 19, 2023 | K220288 | NP Medical nPulse K150 Neutral Displacement Needle Free Connector, nPulse Neutral displacement needle free connector, nPulse K150 Needle Free Connector | FPA | Substantially Equivalent | Np Medical, Inc. | accessdata.fda.gov |
| July 29, 2022 | K212982 | Medispine - Spinal Needle, Glospine - Spinal Needle | BSP | Substantially Equivalent | Global Medikit Limited | accessdata.fda.gov |
| May 28, 2015 | K150513 | Imed Technology Intravascular Administration Set, Imed Technology Extension Set | FPA | Substantially Equivalent | Imed Technology, Inc. | accessdata.fda.gov |
| December 19, 2012 | K121803 | INTRAVASCULAR ADMINISTRATION SET | FPA | Substantially Equivalent | Acta Medical, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Cannula, Surgical, General & Plastic Surgery
- All makers of Introducer, Catheter
- All makers of Set, Administration, Intravascular
- All makers of Tubing, Noninvasive
- All makers of Needle, Conduction, Anesthetic (W/Wo Introducer)
- All makers of System, Blood Collection, Vacuum-Assisted, Manual
Updated July 6, 2026. 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.