JOMEL SEAMS REASONABLE LLC

FDA Device Registration & Listing · Hillside, NJ, US · Registration 3005463575

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
3005463575
FEI Number
3005463575
Entity Name
JOMEL SEAMS REASONABLE LLC
City/State/Country
Hillside, NJ, US
Establishment Address
140 Central Ave, Hillside, NJ 07205, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Jomel Seams Reasonable LLC (Owner Number: 10093940)
Owner / Operator Contact Address
140 Central Ave, Hillside, NJ 07205, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PENS BioWrap Family BioWaveHOME Bio WavePRO GO Rx

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2025-08-14
NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief Neurology Class 2 882.5890 2025-08-14
GXY Electrode, Cutaneous Neurology Class 2 882.1320 2025-08-14
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2025-08-14
LIH Interferential Current Therapy Neurology Class 2 882.5890 2025-08-14
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2025-08-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Jomel Seams Reasonable LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21
K033455 Biomedical Life Systems, Inc. ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 2004-01-15
K810593 Medical Devices, Inc. NEUROPAC ULTRA I 1981-03-13
K070612 Top-Rank Health Care Equipment Co., Ltd. TOP-RANK ADHESIVE ELECTRODE 2007-05-07
K123915 Grass Technologies, an Astro-Med, Inc. Product Gro DE48-PLUS 2013-04-24

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005463575. Last updated year: 2026. Please use registration number 3005463575 when referencing this establishment in official correspondence.
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