Who we are:
As a technology-based Manufacturer, ADM Tronics produces electronic components, assemblies and complete systems on a proprietary and OEM contracted or project basis for customers from diverse industries. A core competency lies in prototype development, reverse-engineering, forensic design, beta development through quantity manufacturing.
ADM Tronics operates an FDA inspected Registered Medical Device Manufacturing facility that is cGMP compliant and produces products that are ETL registered, CE marked and meet or exceed most regulatory and quality requirements. The Company utilizes computerized systems for inventory management, production scheduling, in-process data collection, shipping, lot tracking and regulatory compliance.
ADM Tronics has an experienced dedicated, full-time, on-staff team of researchers, engineers and production employees organized in self-directed work teams for efficient and rapid turn-around of customers projects - from a single piece to thousands. Services include design, reverse-engineering, parts and supplier sourcing, 3D prototyping, both additive and subtractive, beta-manufacturing, contract manufacturing and high-volume scale-up.
These proprietary devices, conceived, designed and produced in-house, include therapeutic and diagnostic medical technologies in fields as diverse as audiology, physical medicine, wound therapy, neurology and urology.
History of innovation:
ADM Tronics Inc. was founded in 1969 by the late Dr. Alphonso DiMino who is regarded by many as a scientific genius of inventions. Dr. DiMino created The Sonotron and The Aurex, both non-invasive electronic therapy technologies. Under his son, Andre’ DiMino, his legacy of innovation continues as ADM Tronics, Inc. researches and develops new technologies. These devices, conceived, designed and produced in-house include therapeutic and diagnostic medical technologies in fields as diverse as audiology, physical medicine, wound therapy, neurology and urology.
We are a registered FDA Medical Device Manufacturing Facility for Class 1, 2 and 3 Devices. We are ISO-13485 certified and proficient in:
GMP/QSR documentation in design
FDA Application submissions for IDE, 510(k)
UL, CE, CMDCAS, JIS