Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2436906

FEI Number

1000521467

Entity Name

POST SURGICAL MFG.

City/State/Country

Hauppauge, NY, US

Establishment Address

25 Plant Ave, Hauppauge, NY 11788, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Post Surgical Mfg. (Owner Number: 10042993)

Owner / Operator Contact Address

25 Plant Avenue, Hauppauge, NY 11788, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bone Gouge MicroAire Chisels and Osteotomes ILS Circular Size Set Skin Curette Bone Curette Ligaclip Clip Applier Bone Elevator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HTE	Elevator	General, Plastic Surgery	Class 1	878.4800	2013-01-29
GDH	Gouge, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2013-01-29
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2013-01-29
KDG	Chisel (Osteotome)	General, Plastic Surgery	Class 1	878.4820	2013-01-24
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2013-01-17
FTY	Tape, Measuring, Rulers And Calipers	General, Plastic Surgery	Class 1	878.4800	2014-12-11
EMF	Knife, Surgical	General, Plastic Surgery	Class 1	878.4800	2014-12-11
FZS	Curette, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2013-01-29
GDO	Applier, Surgical, Clip	General, Plastic Surgery	Class 1	878.4800	2013-01-17
GEG	Elevator, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2013-01-29

Official Correspondent

Bob Gioia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Post Surgical Mfg.

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
K894785	Fdt Precision Machine Co., Inc.	SURGICAL CHISEL/OSTEOTOME	1989-08-18

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.
Z-0034-2012	X Spine Systems Inc	1	Axle Interspinous Fusion System Torque Driver Handle, Model #: X060-0323, Lot # 525941, S/Ns 001-017, Lot # 525942, S/Ns 001-050, Mfr. By: Bradshaw Medical Inc., Kenosha, WI 53144 The Axle Torque Driver Handle is used to lock the set screw into the locking plate.

Similar Registrations

Registration Number	Establishment Name	Location
3007334784	HUAIAN TISURG MEDICAL INSTRUMENTS CO., LTD.	Huaian City Jiangsu, CN
8039053	ULRICH AG	ST. GALLEN Sankt Gallen, CH
3010009693	rms Surgical	Anoka, MN, US
1834379	MICROPULSE INC	Columbia City, IN, US
3009973505	ARCH Medical Solutions - Memphis	BARTLETT, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2436906. Last updated year: 2026. Please use registration number 2436906 when referencing this establishment in official correspondence.