Flyte In-Home Pelvic Floor Treatment

The Pelvital System model MTI-1 is a repeat-use vaginal device for pelvic-floor muscle conditioning and strengthening. The FDA filing describes its use during normal Kegel exercises and…

Registry build 21.09.26

The Pelvital System model MTI-1 is a repeat-use vaginal device for pelvic-floor muscle conditioning and strengthening.

The FDA filing describes its use during normal Kegel exercises and states that it is designed for home training.

Role and Configuration

The system includes an inserted probe and a handheld control unit that provides biofeedback about correct muscle engagement.

The stated purpose is to strengthen pelvic-floor muscles, which the filing says has been found to help women with stress urinary incontinence.

7manufacturers in China registered for this device type
2catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (4), Shanghai (1), Hunan (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HIR
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Dongguan Q & S Electronic Manufacturing Company Limited Dongguan Guangdong Contract manufacturer 5
Suzhou Armocon Technology Co., Ltd. Jiangsu Jiangsu Contract manufacturer 5
Shenzhen MED-Link Electronics Tech Co., Ltd. Shenzhen Guangdong Contract manufacturer 18
Shenzhen Konmed Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Hunan Accurate BIO-Medical Technology Co., Ltd. Changsha Hunan Contract manufacturer 7
Guangdong Yuxiang Silicone & Plastic Co., Ltd. Zhongshan Guangdong Manufacturer 2

Record

Regulatory record for Flyte In-Home Pelvic Floor Treatment
Listed by Pelvital USA, Inc., United States
FDA product code HIR
Device type Perineometer
Device class Class 2
Regulation 21 CFR 884.1425
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K200409
Record published 2021-08-04

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Over the counter Yes
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Flyte In-Home Pelvic Floor Treatment
Catalogue number Size Status
MTI-1 In distribution
MTI-1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pathway Prometheus Group OF NEW Hampshire Limited, THE 7
Peritron Laborie Medical Technologies, Canada ULC 4
Perifit Care+ X6 Innovations 3
Levina ZMI Electronics Ltd. 3
MEP Personal Medical Corp. 2
Perifit X6 Innovations 2
IVS-2 Personal Medical Corp. 2
FemiScan Bittium Biosignals Ltd. 2
SenseRx — Anal/Small Vaginal and Vaginal EMG Personal Medical Corp. 2
Intimate Rose Plus EV Holdings Inc 1
InTone® Nasp Incontrol Medical, LLC 1
InTone® by Viveve Incontrol Medical, LLC 1

Showing 12 of 36. All products under Perineometer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K240805 2024-08-01
K233362 2023-12-29
K212655 2021-09-21
K210764 2021-04-13
K200409 2020-07-10

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer