Seid Medical GmbH

FDA Device Registration & Listing · DENKINGEN Baden-Wurttemberg, DE · Registration 8010523

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
8010523
FEI Number
3006720810
Entity Name
Seid Medical GmbH
City/State/Country
DENKINGEN Baden-Wurttemberg, DE
Establishment Address
Zeppelinstr. 10, DENKINGEN Baden-Wurttemberg 78588, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Seid Medical GmbH (Owner Number: 8010523)
Owner / Operator Contact Address
Zeppelinstr. 10, --, DENKINGEN, DE-BW 78588, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Speculum Trans Speculum

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTF Curette General, Plastic Surgery Class 1 878.4800 2025-11-17
KAE Forceps, Ent Ear, Nose, Throat Class 1 874.4420 2025-11-17
FXE Speculum, Non-Illuminated General, Plastic Surgery Class 1 878.1800 2012-11-08
HWM Osteotome General, Plastic Surgery Class 1 878.4800 2025-11-17
HTR Rasp General, Plastic Surgery Class 1 878.4800 2025-11-17
GAD Retractor General, Plastic Surgery Class 1 878.4800 2015-07-20
GEG Elevator, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2025-04-29
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2024-12-03

Official Correspondent

Eugen Sali

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

Seid Medical 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
K922626 Andronic Devices, Ltd. ADEPT INSTRUMENT POSITIONING ACCESSORY 1992-10-19
K820290 The Anspach Effort, Inc. SELF RETAINING RETRACTOR FOR HAND SURG 1982-03-05
K760422 Cutter Laboratories, Inc. SURGICAL RETRACTOR 1976-08-23
K143738 Intuit Medical Products, LLC DSS Sinusplasty Balloon Catheter 2015-08-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2014 Aesculap, Inc. 1
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010523. Last updated year: 2026. Please use registration number 8010523 when referencing this establishment in official correspondence.
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