FDA 510(k)

MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer

Número K: K241552 · 2024-09-06

Data da decisão2024-09-06

Código do produtoMRD

DecisãoSubstantially Equivalent

Resumo do dispositivo

MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Worldwide, LLC. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K241552. The device is classified under product code MRD. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer?

MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Mentor Worldwide, LLC. The 510(k) number is K241552.

When did MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer receive FDA 510(k) clearance?

MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer received FDA 510(k) clearance on 2024-09-06, under 510(k) number K241552.

Who is the listed applicant for MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer?

The FDA 510(k) record lists Mentor Worldwide, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer?

The FDA product code for MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer is MRD.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Outros registros que listam Mentor Worldwide, LLC como candidato(a)

K242963MENTOR™ PliaForm™ Breast Tissue Expander w/ Suture Tabs K243271MENTOR™ MemoryShape™ Resterilizable Gel Breast Implant Sizer; MENTOR™ MemoryGel™ Resterilizable Gel Breast Implant Sizer; MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer K243836Mentor™ CPX ™ 4 PLUS Enhance Breast Tissue Expander K241918MENTOR™ CPX™4 PLUS Enhance Breast Tissue Expander K182335CPX 4 Breast Tissue Expander with Smooth Surface K161176Expansores de Tissue de Mama ARTOURA com Superfície Lisa

Ver todos os 8 dispositivos →

Dispositivos Relacionados (Código: MRD)

K243271MENTOR™ MemoryShape™ Resterilizable Gel Breast Implant Sizer; MENTOR™ MemoryGel™ Resterilizable Gel Breast Implant Sizer; MENTOR™ MemoryGel™ Enhance Single Use Gel SizerMentor Worldwide, LLC K203229NATRELLE INSPIRA Single Use Sizers for Gel ImplantsAllergan K200706Sientra OPUS Silicone Gel Breast Implant SizerSientra, Inc.K183163Intraoperative, Single-Use, Sterile, Silicone Breast Sizer Motiva Implant MatrixMotiva USA, LLC

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.