Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011111237

FEI Number

3011111237

Entity Name

AMERICAN SURGICAL SPECIALTIES COMPANY

City/State/Country

Nashville, TN, US

Establishment Address

475 Metroplex Drive, Suite 401, Nashville, TN 37211, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

AMERICAN SURGICAL SPECIALTIES COMPANY (Owner Number: 10087236)

Owner / Operator Contact Address

475 Metroplex Drive, Suite 401, Nashville, TN 37211, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AmeriSurg Amerisurg Amerisurg AMERISURG

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDC	Instrument, Surgical, Disposable	General, Plastic Surgery	Class 1	878.4800	2024-11-18
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2023-01-31
JEA	Table, Surgical With Orthopedic Accessories, Ac-Powered	General, Plastic Surgery	Class 1	878.4960	2023-01-31
LRC	Instrument, Ent Manual Surgical	Ear, Nose, Throat	Class 1	874.4420	2024-11-18

Official Correspondent

LAURIE DOBBS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AMERICAN SURGICAL SPECIALTIES COMPANY

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
K831798	I M, Inc.	DISPOSABLE SCALPELS	1983-07-19
K143738	Intuit Medical Products, LLC	DSS Sinusplasty Balloon Catheter	2015-08-27

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

Registration Number	Establishment Name	Location
1043646	Medegen Medical Products	GALLAWAY, TN, US
3013298431	VEENAK INTERNATIONAL LIMITED	BIRMINGHAM, GB
3002834291	MIAN SHAHID CORP.	MUZAFFAR PUR, SIALKOT Punjab, PK
3009750712	Quiroproductos de Cuauhtemoc S. De R.L. de C.V.	Cuauhtemoc Chihuahua, MX
1820334	Cook Incorporated	Bloomington, IN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011111237. Last updated year: 2026. Please use registration number 3011111237 when referencing this establishment in official correspondence.