MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-05-14 for ASTRON CLEARSPLINTS NI manufactured by Prismatik Dentalcraft, Inc..
[145076907]
Follow-up attempts were made to obtain the event information and product return; however, there has been no response from the clinic. Once new information is obtained and evaluation is completed, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10
[145076908]
It was reported that a patient experienced an allergic reaction after using an astron clearsplint nightguard. The patient reported having burning sensation on the tongue shortly after wearing the nightguard.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3011649314-2019-00151 |
MDR Report Key | 8610379 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-05-14 |
Date of Report | 2019-12-02 |
Date Mfgr Received | 2019-10-17 |
Device Manufacturer Date | 2019-03-16 |
Date Added to Maude | 2019-05-14 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | DENTIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. TOAN HOANG |
Manufacturer Street | 2212 DUPONT DRIVE SUITE P |
Manufacturer City | IRVINE CA 92612 |
Manufacturer Country | US |
Manufacturer Postal | 92612 |
Manufacturer Phone | 9492251235 |
Manufacturer G1 | PRISMATIK DENTALCRAFT, INC. |
Manufacturer Street | 2212 DUPONT DRIVE SUITE P |
Manufacturer City | IRVINE CA 92612 |
Manufacturer Country | US |
Manufacturer Postal Code | 92612 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ASTRON CLEARSPLINTS |
Generic Name | NIGHTGUARD, ASTRON SPLINT |
Product Code | MQC |
Date Received | 2019-05-14 |
Model Number | NI |
Catalog Number | NI |
Lot Number | NI |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PRISMATIK DENTALCRAFT, INC. |
Manufacturer Address | 2212 DUPONT DRIVE SUITE P IRVINE CA 92612 US 92612 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-05-14 |