Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1222188

FEI Number

1222188

Entity Name

LIFE INSTRUMENT CORP.

City/State/Country

BRAINTREE, MA, US

Establishment Address

91 French Ave, BRAINTREE, MA 02184, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

LIFE INSTRUMENT CORP. (Owner Number: 9001270)

Owner / Operator Contact Address

91 French Avenue, --, Braintree, MA 02184, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Scalpel Holder Knife Blade Holder Chisels Markers Mallets Rongeurs Forceps Tamps Elevators Gouges Curettes Osteotomes Funnel Retractors Suction Tubes MALLET ELEVATOR Endplate Rasp Cervical Endplate Rasp OSTEOTOME TAMP Suction Tubes Retractors Curettes Mallets Osteotomes Forceps Tamps Gouges Chisels Rongeurs Markers Elevators Micro Bayonet Nerve Hook Micro Nerve Hook Bayonet Nerve Hook White Russian Forcep Micro Forceps IVD Forceps Bayonet Bipolar Forcep Jefferson Forcep Bayonet Micro Scissors Micro Scissors Murphy Ball Probe Ball Probe Flxible Ball Probe Bayonet Ball Probe Micro Ball Probe Long Handle Insert Spine Dissection Sterilization Tray Outer Sterilization Case Micro Curete Sterilization Tray Cobb Instrument Rack Micro Curette Insert American Curette/Osteotome Insert Sterilizable Storage Tray Sterilization Insert Long Handle Sterilization Tray Pattie Tray Micro Rainbow Curettes O'Brien Curettes Down Pushing Curette Cone Ring Curettes Cobb Curettes American Rainbow Curettes Brun Curettes Charnley Curettes Thoracic Curettes Micro Curette Triangle Endplate Curette Micro Axial Curette Teardrop Curettes Navicular Gouge Gouges Long Gouges Piggot Gouges Capener Lamina Gouge Hibbs Gouges Ferret Gouge Harvesting Gouge Smith Peterson Gouges Stencil Guide RETRACTOR

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GDZ	Handle, Scalpel	General, Plastic Surgery	Class 1	878.4800	2009-11-05
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2012-05-21
GFJ	Mallet, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2001-11-21
HTE	Elevator	General, Plastic Surgery	Class 1	878.4800	2001-11-21
HTR	Rasp	General, Plastic Surgery	Class 1	878.4800	2012-02-01
HWM	Osteotome	General, Plastic Surgery	Class 1	878.4800	2001-11-21
HXG	Tamp	Orthopedic	Class 1	888.4540	2001-11-21
HAO	Instrument, Surgical, Non-Powered	Neurology	Class 1	882.4535	2012-05-21
GDG	Hook, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2009-11-05
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2009-11-05
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2009-11-05
HXB	Probe	Orthopedic	Class 1	888.4540	2009-11-05
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2009-11-05
FZS	Curette, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2001-11-21
GDH	Gouge, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2001-11-21
FZX	Guide, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2025-02-04
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2001-11-21

Official Correspondent

Joanne Luca

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIFE INSTRUMENT CORP.

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
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02
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

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0039-2018	Teleflex Medical	1	Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
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.
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 1222188. Last updated year: 2026. Please use registration number 1222188 when referencing this establishment in official correspondence.