Transtimulation Research Inc

FDA Device Registration & Listing · Pasadena, CA, US · Registration 3036040187

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3036040187
FEI Number
3036040187
Entity Name
Transtimulation Research Inc
City/State/Country
Pasadena, CA, US
Establishment Address
898 N Fair Oaks Ave, Unit C, Pasadena, CA 91103, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Transtimulation Research, Inc (Owner Number: 10092672)
Owner / Operator Contact Address
420 S Madison Ave, Apt 206, Pasadena, CA 91101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230526
PMA Number
N/A

All Registered Proprietary Names

Patch-TEA TEA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2026-06-18
QHH Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs) Gastroenterology, Urology Class 2 876.5340 2025-02-04

Official Correspondent

Victor Pikov

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Transtimulation Research, Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3029924973 SHENZHEN SINREL TECH LTD Shenzhen Guangdong, CN
3003255790 WITKO INCORPORATED Wolcott, IN, US
3038295706 JUST KEEP HEALTHY CO., LTD. Samkkei Munichay District Kampong Speu, KH
3011562129 MIRAE MEDI&TECH CO., LTD. Cheonan-si Chungnam, KR
3005170249 Shenzhen Dongdixin Technology Co., Ltd. SHENZHEN Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3036040187. Last updated year: 2026. Please use registration number 3036040187 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.