OMT, LLC

FDA Device Registration & Listing · Fort Lauderdale, FL, US · Registration 3005663073

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
3005663073
FEI Number
3005663073
Entity Name
OMT, LLC
City/State/Country
Fort Lauderdale, FL, US
Establishment Address
3848 SW 30th Ave, Fort Lauderdale, FL 33312, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
OMT, LLC (Owner Number: 9085200)
Owner / Operator Contact Address
3848 S.W. 30TH AVE., --, Ft Lauderdale, FL 33312, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kerrisons Pattie / Neuropatties Cranial Dissectors - Microsurgical STERICYL's Silicon Brain Spatulas

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTX Rongeur Orthopedic Class 1 888.4540 2018-02-08
HBA Neurosurgical Paddie Neurology Class 2 882.4700 2006-03-31
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2018-02-08
GDY Gauze/Sponge, Internal, X-Ray Detectable General, Plastic Surgery Class 1 878.4450 2017-12-26
EFQ Gauze/Sponge, Internal Unknown Class U N/A 2017-12-26
GAF Spatula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2018-02-08

Official Correspondent

MONIQUE TRAAD

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OMT, 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
K790050 Stanford Professional Products SPONGES, STANFORD STERILE LAP 1979-01-17
K861444 Surgical Specialties, Inc. S1 NASAL PACKING 1986-05-06
K863737 Hermitage Hospital Products, Inc. SPONGES STERILE TWIN PAKT AND SINGLES 1986-10-14
K940351 Certified Safety Mfg., Inc. EXTRA LARGE COMPRESS DRESSING 1994-02-25
K950404 Lockett Medical Corp. LOCKETT MEDICAL CORP. GAUZE 1995-04-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005663073. Last updated year: 2026. Please use registration number 3005663073 when referencing this establishment in official correspondence.
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