Mar 04, 2022
A global dental prosthetics maker envisioned a new method for identifying and tracking dentures, from the point of manufacture at the lab to end-use among residents at nursing homes and other care facilities. While 23 US states currently require some form of physical user identification on each denture, compliance has typically been deficient. The reason is that the added costs associated with engraving patient names on the dentures and a user’s typical reluctance to reveal themselves as a denture wearer.
In nursing facilities, because most dentures lack user names, it’s often difficult to match individuals with their dentures after they’ve been routinely collected for cleaning and maintenance or misplaced. These facilities also face potential HIPAA medical confidentiality violations if a labeled denture is mishandled and user identity is exposed beyond facility personnel. With the high costs of custom-made dentures and their day-to-day necessity for the user, this common problem called out for an innovative technical remedy.
The client looked at embedding miniature passive RFID tags into a denture, which could be wirelessly scanned, logged, and identified via a custom software app. They initially discussed this idea with us at a medical device tradeshow after learning of our past success with RFID tags, smaller and medical-grade tags combined with our own readers and software across multiple mobile tracking applications. Our product team then set about developing the necessary hardware and software to the customer’s specifications. Bringing the convenience of RFID technology to dentures meant tackling several unique requirements:
Scanned dentures would be automatically linked to the client’s custom-developed proprietary website database, enabling dentists, labs, and patients to authenticate dentures via a three-part digital certificate containing every product unit’s unique identifier (UID) along with important patient data.
Following a detailed analysis of the technical specifications, our hardware engineering team developed the optimal tag and reader combination. They determined a 5 mm epoxy-encapsulated ISO 15693 HF tag would withstand the long-term conditions of dental use and maintenance. These tags were paired with our standard plug-and-play USB RFID reader. We simultaneously assembled an in-house software team to execute the web and mobile app development and quality assurance for the client’s dentures ID solution. Our software team custom-designed the corresponding denture app.
The digital UID certificate formats were created using Microsoft .net 4.0 and SQL server development platforms without farming out software programming to a third-party vendor. QA included peer reviews, code reviews, and custom test development, along with regular project audits. Our software engineers recognized compatibility issues with later models of some name-brand smartphones during our initial project testing. The problem was traced to those phones’ internal wireless charging system, which blocked RFID reception.
To adopt this solution into a universal option for all mobile devices, our hardware team suggested including an NFC tag alongside the original ISO 15693 tag, which could prove equally readable by all mobile devices. Our software team devoted an additional three months to adapting a downloadable Android mobile app that could utilize the low-power NFC readers built into those devices. “The universal readability of the RFID chips is what makes this application so appealing. The real promise is that it’ll significantly reduce labor costs at the dental labs, and this will be a major selling point the labs can offer to dentists. We believe this represents a real milestone in the industry,” said the Company’s CEO.
Following successful prototyping and initial DFM planning for this innovative RFID denture ID solution, the client shepherded the system components through the FDA 510(k) premarket approval process for oral products. As RFID-based denture identification was essentially a new product category, the FDA required an especially lengthy and comprehensive series of applications, committee proceedings, and other administrative hurdles. Following final FDA clearance in October 2017, the client gave us the formal go-ahead for a full production order. Tags packaged with digital certificate instructions for dental labs.
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Our flagship Chennai location opened in 2006 and lies within a Special Economic Zone (SEZ) for electronics manufacturing, offering economic incentives for imports and exports. This primary facility is within 90 minutes of the Chennai seaport and 20 minutes to the international airport. Additional road and rail connectivity links to the rest of India and beyond and infrastructure advantages with faster import and export clearances. We also have labor force flexibility, both technical and manual, to scale to demand rapidly.
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