AESCULAP, INC.

FDA Device Registration & Listing · HAZELWOOD, MO, US · Registration 3003587896

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
3003587896
FEI Number
3003587896
Entity Name
AESCULAP, INC.
City/State/Country
HAZELWOOD, MO, US
Establishment Address
615 LAMBERT POINTE DR., HAZELWOOD, MO 63042, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
AESCULAP, INC. (Owner Number: 2916714)
Owner / Operator Contact Address
3773 CORPORATE PKWY., --, Center Valley, PA 18034, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RETRACTOR Aesculap

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JEY Plate, Bone Dental Class 2 872.4760 2008-06-02
GAD Retractor General, Plastic Surgery Class 1 878.4800 1989-11-27
GFD Dermatome General, Plastic Surgery Class 1 878.4820 2008-07-08

Official Correspondent

Kamaal Anas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AESCULAP, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2916714 AESCULAP, INC. CENTER VALLEY, PA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K172572 Stryker Stryker Upper-Face AXS screws and Mid-Face AXS screws 2017-10-31
K121589 Biomet Microfixation BIOMET MICROFIXATION FACIAL PLATING SYSTEM 2012-09-21
K984230 Osteogenics Biomedical, Inc. OSTEO-MESH TM-300 1999-02-04
K021618 Osteomed Corp. OSA RIGID INTERNAL FIXATION SYSTEM 2002-08-08
K922626 Andronic Devices, Ltd. ADEPT INSTRUMENT POSITIONING ACCESSORY 1992-10-19

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0043-2007 Bioplate Inc 2
Bioplate Resorbable Bone Fixation Tack, Catalog Number: 89-0120, Item Number: SG#-45
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 3003587896. Last updated year: 2026. Please use registration number 3003587896 when referencing this establishment in official correspondence.
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