Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010892271

FEI Number

3010892271

Entity Name

FEMSelect Ltd

City/State/Country

Modi'in Central, IL

Establishment Address

HaMa'ayan 2, First Floor, Modi'in Central 7177871, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

FEMSelect Ltd (Owner Number: 10053647)

Owner / Operator Contact Address

HaMa'ayan 2, First Floor, Modi'in, IL-NOTA 7177871, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K160569

PMA Number

N/A

All Registered Proprietary Names

EnPlace

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PBQ	Fixation, Non-Absorbable Or Absorbable, For Pelvic Use	Obstetrics/Gynecology	Class 2	884.4530	2016-12-27

Official Correspondent

Deborah Garner

US Agent Details

Matt Dryden Business: ProMedic, LLC Email: matt.dryden@promedic.cc Phone: (239) 3076063

Related Public Records

Same Entity

FEMSelect Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010892271. Last updated year: 2026. Please use registration number 3010892271 when referencing this establishment in official correspondence.