Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
None linked.
Manufacturer compliance record
None in the loaded window.
Similar devices
- 900-001 Anatomical Chin Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-002 Symmetrical Chin Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-003 Bilateral Groove Chin Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-004 Articulated Chin Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-005 Cleft Chin Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-006 Concave Chin Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-007 Curvilinear Chin Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-008 Mittleman Geniomandibular Groove Chin/Jowl Sizer Set IMPLANTECH ASSOCIATES, INC.
- 900-009 Mittleman Geniomandibular Groove Jowl Sizer Set IMPLANTECH ASSOCIATES, INC.
- Anatomical Chin IMPLANTECH ASSOCIATES, INC.
- Anatomical Chin IMPLANTECH ASSOCIATES, INC.
- Anatomical Chin IMPLANTECH ASSOCIATES, INC.
Select up to two to place side-by-side with this device.