OPTP LLC

FDA Device Registration & Listing · Minneapolis, MN, US · Registration 2131610

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
2131610
FEI Number
1000115925
Entity Name
OPTP LLC
City/State/Country
Minneapolis, MN, US
Establishment Address
3800 Annapolis Ln N Ste 165, Minneapolis, MN 55447, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
OPTP LLC (Owner Number: 9004259)
Owner / Operator Contact Address
3800 ANNAPOLIS LN.#165, --, Minneapolis, MN 55447, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Back Vitalizer OPTP Mobilization Wedge Original Kaltenborn Concept Wedge Original Norsk Mobilization Wedge OPTP Joint Distractor Endura Taping Kit Endura Fix Tape Endura Sports Tape

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ION Exerciser, Non-Measuring Physical Medicine Class 1 890.5370 1994-01-26
IOD Components, Exercise Physical Medicine Class 1 890.5350 2016-08-11
HXT Tape, Orthopedic General, Plastic Surgery Class 1 878.4800 2016-01-11

Official Correspondent

Catherine Lindvall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OPTP LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2131610. Last updated year: 2026. Please use registration number 2131610 when referencing this establishment in official correspondence.
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