Reflex Group

FDA Device Registration & Listing · Oceanside, CA, US · Registration 3009130317

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
3009130317
FEI Number
3009130317
Entity Name
Reflex Group
City/State/Country
Oceanside, CA, US
Establishment Address
530 S Coast Hwy, Oceanside, CA 92054, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device
Owner / Operator
ReflexGroup (Owner Number: 10037789)
Owner / Operator Contact Address
530 South Coast Highway, Oceanside, CA 92054, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Trizone Ankle Brace Reaction Sleeve, OA Reaction Sleeve, A22 Sleeve, OA Reaction Trifit Sleeve SAEBOSTRETCH, SAEBOGLOVE, SAEBOFLEX, SAEBOREACH EMBRACE360 Trizone Webtech OA Reaction OA Reaction Trifit Reaction Knee Brace Nordt Knee Brace

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITW Joint, Ankle, External Brace Physical Medicine Class 1 890.3475 2016-12-13
IPM Cover, Limb Physical Medicine Class 1 890.3025 2017-01-24
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2014-07-11
EFW Toothbrush, Manual Dental Class 1 872.6855 2016-12-14
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2011-08-16

Official Correspondent

Ian Kovacevich

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ReflexGroup
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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009130317. Last updated year: 2026. Please use registration number 3009130317 when referencing this establishment in official correspondence.
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