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Sign in to claim this brandPRECISION MEDICAL, INC.
United States·US-MF-000008706
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 300, Held Drive, Northampton, United States
- Website
- precisionmedical.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Brian Klotz
- EUDAMED SRN
- US-MF-000008706
- FDA FEI Number
- 2523148
- DUNS Number
- —
Catalogue (196)
Page 1 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 1MFA Flowmeters | 1MFA Air Series | FDA UDI | Class I | Unknown |
| Vacuum Regulator | PM3300HV series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM5950 | FDA UDI | Class II | Active |
| Precision Medical | PMX3100 | FDA UDI | Class II | Active |
| Vacuum Regulator | PM3300 series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM9100 SERIES | FDA UDI | Class II | Active |
| Vacuum Regulator | PS3400D series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM3500 SERIES | FDA UDI | Class II | Active |
| HeliO2 Blender | PM5580 | FDA UDI | Class II | Active |
| Precision Medical | PMX3500D | FDA UDI | Class II | Active |
| Vacuum Regulator | PM3300D series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM3300 SERIES | FDA UDI | Class II | Active |
| Precision Medical | PMX3500 | FDA UDI | Class II | Active |
| Easy Comp Compressor | PM15 SERIES | FDA UDI | Class II | Active |
| Vacuum Regulator | PM3300HV series w/PM9100 & Vac Trap | FDA UDI | Class II | Active |
| Precision Medical | PMX9000-50 | FDA UDI | Class II | Unknown |
| Precision Medical Inc. | 1901-76301 | FDA UDI | Class II | Unknown |
| Precision Medical Inc. | PM65 | FDA UDI | Class II | Active |
| Dial Flowmeter | 7MFA O2 SERIES | FDA UDI | Class I | Active |
| Easy Pulse 5 Oxygen Conserving Regulator | 198712 | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM4130 | FDA UDI | Class II | Active |
| Vacuum Regulator | PS3300D series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM3100D SERIES | FDA UDI | Class II | Active |
| Precision Medical Inc. | PS3400 | FDA UDI | Class II | Active |
| Vacuum Regulator | PM3100DHVBM | FDA UDI | Class II | Unknown |
| Vacuum Regulator | PM3300HV series w/PM9100 | FDA UDI | Class II | Active |
| Precision Medical | 502519-10 | FDA UDI | Class II | Active |
| HeliO2 Blender | PM5480 | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM61 | FDA UDI | Class II | Active |
| 1MFA Flowmeters | 1MFA1001MOD | FDA UDI | Class I | Active |
| Easy Dial Reg | 1687 Dial Series | FDA UDI | Class I | Active |
| Precision Medical Inc. | PM63E | FDA UDI | Class II | Active |
| Vacuum Regulator | PM3100HV series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM5900DRW | FDA UDI | Class II | Active |
| Precision Medical | 502519-20 | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM4150 | FDA UDI | Class II | Active |
| Vacuum Regulator | PS3100D | FDA UDI | Class II | Unknown |
| Vacuum Regulator | PM3400D SERIES | FDA UDI | Class II | Active |
| Vacuum Regulator | PS3000D | FDA UDI | Class II | Unknown |
| PRECISION ECO™ Plant Based Procedural Mask with Earloops | CW005 | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM3600EPCME | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM3000D SERIES | FDA UDI | Class II | Active |
| Precision Medical Inc. | PS3100 SERIES | FDA UDI | Class II | Active |
| Vacuum Regulator | PM300HV series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM3200E SERIES | FDA UDI | Class II | Active |
| Precision Medical Inc. | PM500 | FDA UDI | Class II | Active |
| PRECISION ECO™ Compostable Procedural Mask with Earloops | CW002 | FDA UDI | Class II | Active |
| Precision Medical Inc. | PS3000HV SERIES | FDA UDI | Class II | Active |
| Vacuum Regulator | PM3400 series w/ Vac Trap | FDA UDI | Class II | Active |
| Precision Medical | PMX9000 | FDA UDI | Class II | Unknown |
Related Companies
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FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 8, 2015 | Z-0272-2016 | — | terminated | These lots of Oxygen Dial Regulators could have the settings label off by one position. When the indicator arrow points to OFF position, the regulator is actually on the half liter setting (0.50), for the 15 liter. For the 8 liter, instead of being in the OFF position, the regulator will be in the quarter liter setting (0.25). |
| Mar 5, 2010 | Z-1561-2010 | — | terminated | The on/off outlet is mislabeled so that when a user/operator turns selector to "on", it actually may be turned "off" |
| Oct 4, 2006 | Z-0153-2007 | — | terminated | Component assembly; The fill chuck is not assembled properly which may allow the device to come apart over time releasing its contents. |
| Nov 9, 2004 | Z-0307-05 | — | terminated | Battery charger can be overcharged and overheat |
| Nov 9, 2004 | Z-0308-05 | — | terminated | Battery charger can be overcharged and overheat |