MTT GMBH

FDA Device Registration & Listing · Lueneburg Lower Saxony, DE · Registration 3011545155

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
3011545155
FEI Number
3011545155
Entity Name
MTT GMBH
City/State/Country
Lueneburg Lower Saxony, DE
Establishment Address
Boecklerstr. 26, Lueneburg Lower Saxony 21339, DE
Establishment Type(s)
Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
MTT GmbH (Owner Number: 10048443)
Owner / Operator Contact Address
Boecklerstr. 26, Lüneburg, DE-NI 21339, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PeriGrid Reusable Stepper A-TP Solidlock Positioning PeriGrid HDR Single Use Disposable Template Stainless Steel Template Stepper B PeriGrid Disposable Probe receptacle (SB) SIUI ECBP (ACCESSORY to Stepper) SolidLock F SolidLock HS-500ext SolidLock HS Wolf Endomotion System SolidLock F-500ext

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IWJ System, Applicator, Radionuclide, Manual Radiology Class 1 892.5650 2021-11-03
KOA Surgical Instruments, G-U, Manual (And Accessories) Gastroenterology, Urology Class 1 876.4730 2021-11-03

Official Correspondent

Stefan Renckly

US Agent Details

Kirby Rust Business: DK North America LLC Email: krust@dknorthamerica.com Phone: (404) 9849400

Related Public Records

Same Entity

MTT GmbH
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
K973037 Avid N.I.T., Inc. N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000 1998-01-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0040-2012 Worldwide Medical Technologies, LLC 1
Prostrate Seeding Applicator Needle. Product code PSS1820AT Packed in boxes of (25) with five Single Packs and four five packs or as singles or five packs. Worldwide Medical Technologies, LLC Used to introduce radionuclide seeds of 1-125 or Pd-103 into the body for radiation therapy. This device is typically used in the transperineal approach for placing radionuclide seeds in the prostate

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2523676 B. BRAUN US DEVICE MANUFACTURING LLC ALLENTOWN, PA, US
1120804 BEST MEDICAL INTERNATIONAL, INC. SPRINGFIELD, VA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011545155. Last updated year: 2026. Please use registration number 3011545155 when referencing this establishment in official correspondence.
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