• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: RANIR LLC REST ASSURED MOUTH GUARD; RA GEN II MOUTH GUARD

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

RANIR LLC REST ASSURED MOUTH GUARD; RA GEN II MOUTH GUARD Back to Search Results
Device Problem Split (2537)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 04/10/2015
Event Type  malfunction  
Event Description
The consumer stated that the bottoms of the mouthguards are splitting.
 
Manufacturer Narrative
Device not returned to manufacturer.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
REST ASSURED MOUTH GUARD
Type of Device
RA GEN II MOUTH GUARD
Manufacturer (Section D)
RANIR LLC
4701 east paris se
grand rapids MI 49512 535
Manufacturer (Section G)
RANIR LLC
4701 east paris se
grand rapids MI 49512 535
Manufacturer Contact
elsa baker
4701 east paris ave se
grand rapids, MI 49512-5353
6166988880
MDR Report Key4761096
MDR Text Key5782616
Report Number1825660-2015-00061
Device Sequence Number1
Product Code OBR
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Device Unattended
Remedial Action Replace
Type of Report Initial
Report Date 05/10/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/09/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator Device Unattended
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received04/10/2015
Was Device Evaluated by Manufacturer? No
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
-
-