SMART RECOVERY TECHNOLOGIES LLC

FDA Device Registration & Listing · Quakertown, PA, US · Registration 3012176966

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
3012176966
FEI Number
3012176966
Entity Name
SMART RECOVERY TECHNOLOGIES LLC
City/State/Country
Quakertown, PA, US
Establishment Address
2070 angstadt road, Quakertown, PA 18951, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Smart Recovery Technologies Llc (Owner Number: 10082736)
Owner / Operator Contact Address
2070 Angstadt Rd, Quakertown, PA 18951, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K212169
PMA Number
N/A

All Registered Proprietary Names

Smart Stim; Transcutaneous Electrical Nerve Stimulator Model KTR -2492 Triad 3LT Smart Ice Smart-Wave: Transcutaneous and ESTIM Smart-DVT

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 2024-01-28
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2024-04-16
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2025-02-01
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2025-02-01
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2024-04-09
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2024-04-09
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2023-10-03

Official Correspondent

James Molinaro

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Smart Recovery Technologies 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
K242140 Jiale Health Technology Shenzhen Co., Ltd. Air Compression Leg Massager (K-705) 2025-03-17
K221200 Xbody Hungary Kft. XBody Go USA, XBody Pro USA 2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012176966. Last updated year: 2026. Please use registration number 3012176966 when referencing this establishment in official correspondence.
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