And Matt on your second question regarding potential canaloplasty entrants. I think a couple of things come to mind, maybe four things. Number one is R&D, and I'll get into -- we are the pioneers of ab interno canaloplasty, ab interno canaloplasty, and trabeculotomy. We've been at it for many, many years and have been iterating. So the clinical excellence that is OMNI is the result of tens of thousands of cases, significant clinician feedback, significant iteration. I can tell you it's been a long road to get to the device that we have today that is delivering such incredible results for surgeons and their patients. So it's not easy. So generating a prototype, showing a prototype, maybe even getting a clearance may be straightforward. But delivering a highly dependable reproducible canaloplasty device that is capable of consistently helping the surgeon circumnavigate 100, 200-micron diameter delicate canal for 36 to 40 millimeters around consistently is not easy, period. On the clinical front, I haven't seen -- I personally haven't seen any clinical data from anybody on another ab interno canaloplasty entrant. I think if we're going to be talking about canaloplasty and labels, I think we need to see clinical data, I think it brings us to the third point from a regulatory perspective. I would ask whichever companies or products that we're discussing here. I would ask them what is the indication for use? Is it for canaloplasty? Is it for pressure lowering? Is it for primary open-angle glaucoma? Because I'm pretty sure the pathway that we've gone through requires significant clinical data to be -- to have a canaloplasty indication and to promote for canaloplasty and I mean, we have -- we just announced earlier today, maybe some of you have seen it, we put out a press release just before this call on our IDE for a canaloplasty alone indication. So we have a very large MIGS trial, I think the largest that will ever be conducted, 459 patients, to seek this canaloplasty alone indication. And then lastly, beyond R&D, clinical and regulatory, again, I don't -- I haven't seen any of these devices, but I will say, we've been at this for over a decade, and we have a very broad and deep patent estate intellectual property covering methods and devices of circumferential canalicular glaucoma surgery. So those are the four things that come to mind as it relates to any potential entrants.