MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2000-02-10 for TRANSCEND CERAMIC BRACKET 6001-701, 6001-702 manufactured by 3m Unitek.
[176559]
Orthodontist reported that during the debonding of transcend ceramic brackets, chipping of enamel into dentin occurred on teeth #8 and #9.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2020467-2000-00001 |
| MDR Report Key | 262034 |
| Report Source | 05 |
| Date Received | 2000-02-10 |
| Date of Report | 2000-02-02 |
| Date of Event | 1999-04-20 |
| Date Mfgr Received | 2000-02-02 |
| Date Added to Maude | 2000-02-15 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 0 |
| Manufacturer Contact | MARLYN SCHEFF |
| Manufacturer Street | 2724 SOUTH PECK RD |
| Manufacturer City | MONROVIA CA 91016 |
| Manufacturer Country | US |
| Manufacturer Postal | 91016 |
| Manufacturer Phone | 6265744496 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | TRANSCEND CERAMIC BRACKET |
| Generic Name | ORTHODONTIC BRACKET |
| Product Code | DYW |
| Date Received | 2000-02-10 |
| Model Number | NA |
| Catalog Number | 6001-701, 6001-702 |
| Lot Number | UNK |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 253786 |
| Manufacturer | 3M UNITEK |
| Manufacturer Address | 2724 SOUTH PECK RD. MONROVIA CA 91016 US |
| Baseline Brand Name | TRANSCEND CERAMIC BRACKET |
| Baseline Generic Name | ORTHODONTIC BRACKET |
| Baseline Model No | NA |
| Baseline Catalog No | 6001-701, 6001-702 |
| Baseline ID | NA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 5 | 1. Required No Informationntervention | 2000-02-10 |