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Pharmaceutical Innovations, Inc.

Last updated May 30, 2026

Information

Country: US
Address: —
Website: pharminnovations.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 973-242-2900
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 067486548

Catalogue (74)

Page 2 of 2

Device	Model / Reference	Registries	Class	Status
Pharmaceutical Innovations	UltraPhonic Scanning Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	Lectron III Chloride 10 Electrode Conductivity Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	UltraPhonic Focus Gel Pad	FDA UDI	Class II	Active
Pharmaceutical Innovations	Prep Trode Gentle Conductive Electrode Skin Preparation	FDA UDI	Class II	Active
Pharmaceutical Innovations	TAC GEL Electrically Conductive Adhesive	FDA UDI	Class II	Active
Pharmaceutical Innovations	PI SPRAY Ultrasound Cleaning Solution	FDA UDI	Class I	Active
Pharmaceutical Innovations	VetGel Veterinary Ultrasound Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	Lectron III Chloride 10 Electrode Conductivity Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	Q.R. Quick Recovery Defibrillator Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	LECTRON II Electrode Conductivity Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	TAC GEL Electrically Conductive Adhesive	FDA UDI	Class II	Active
Pharmaceutical Innovations	Prep Trode Gentle Conductive Electrode Skin Preparation	FDA UDI	Class II	Active
Pharmaceutical Innovations	UltraPhonic Conductivity Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	UltraPhonic Focus Gel Pad	FDA UDI	Class II	Active
Pharmaceutical Innovations	ElectroMist Electrolyte Spray	FDA UDI	Class II	Active
Pharmaceutical Innovations	Lectron III Chloride 2 Electrode Conductivity Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	GAMMA Massage & Ultrasound Gel	FDA UDI	Class II	Active
Pharmaceutical Innovations	UltraWarmer Gel Warmer - Red	FDA UDI	Class I	Active
Pharmaceutical Innovations	Prep N Stay Anti-Diaphoretic Skin Preparation	FDA UDI	Class II	Active
Evron Gel	K961222	FDA 510(k)	Class I	Active
Ultra/Phonic Conductivity Gel	K163024	FDA 510(k)	Class II	Active
Ultra/Phonic Scanning Gel	K163026	FDA 510(k)	Class II	Active
Ultra/Phonic Free Conductivity Gel	K163027	FDA 510(k)	Class II	Active
Other-Sonic Transmission Gel	K163023	FDA 510(k)	Class II	Active

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Authorities

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FDA Recalls (8)

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
Aug 13, 2020	Z-2830-2020	—	terminated	The firm registered the product as a Class I device, but has since been informed by FDA that the device is not Class I and requires a 510(k) submission.
Jun 19, 2019	Z-1972-2019	—	terminated	Potential for failed stability antimicrobial effectiveness testing.
Jun 19, 2019	Z-1970-2019	—	terminated	Potential for failed stability antimicrobial effectiveness testing.
Jun 19, 2019	Z-1971-2019	—	terminated	Potential for failed stability antimicrobial effectiveness testing.
Jun 19, 2019	Z-1968-2019	—	terminated	Potential for failed stability antimicrobial effectiveness testing.
Jun 19, 2019	Z-1969-2019	—	terminated	Potential for failed stability antimicrobial effectiveness testing.
Mar 2, 2012	Z-1652-2012	—	terminated	Other-Sonic GENERIC ULTRASOUND TRANSMISSION GEL is being recalled due to possible microbial contamination. An FDA Safety Communication was issued for this product on April 18, 2012.
Mar 2, 2012	Z-1653-2012	—	terminated	Other-Sonic GENERIC ULTRASOUND TRANSMISSION GEL is being recalled due to possible microbial contamination. An FDA Safety Communication was issued for this product on April 18, 2012.