Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010553238

FEI Number

3010553238

Entity Name

RIDGE & CREST COMPANY

City/State/Country

Monterey Park, CA, US

Establishment Address

733 Ridgecrest Street, Monterey Park, CA 91754, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Ridge & Crest Co. (Owner Number: 10045197)

Owner / Operator Contact Address

733 Ridgecrest St., Monterey Park, CA 91754, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Loop&Shear Thread Flexible Surgical Sawing/Dissecting Thread Flexible Surgical Sawing/Dissecting Wire Loop&Shear Ultra Minimally Invasive Thread Dissector Loop&Shear Thread Dissecting Kit Needle Guide LR II Saw Wire GuoPercutaneousWire Zero Bend Radius Wire Saw Flexible Surgical Dissecting/Sawing Wire Wire Saw Gigli Saw Gigli Soft Wire Loop&Shear Kit Loop&Shear Thread Dissector Loop&Shear Thread Dissecting Kit Sciensor II Scissor Retriever II Retractor GuoPercutaneousWire Clamp

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GDI	Dissector, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2014-01-23
GDF	Guide, Needle, Surgical	General, Plastic Surgery	Class 1	878.4800	2013-11-15
GDR	Saw, Manual And Accessories	General, Plastic Surgery	Class 1	878.4800	2013-10-28
HRR	Scissors, Orthopedic, Surgical	Orthopedic	Class 1	888.4540	2013-10-28
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2013-10-28
GFA	Blade, Saw, General & Plastic Surgery, Surgical	General, Plastic Surgery	Class 1	878.4820	2014-01-27
GDJ	Clamp, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2013-10-28

Official Correspondent

Joseph Guo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ridge & Crest Co.

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
K953012	Boston Surgical Products, Inc.	DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLS	1995-07-12

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.

Similar Registrations

Registration Number	Establishment Name	Location
3031562618	Aliform B.V.	Maastricht Limburg, NL
3003244954	ZEPF MEDICAL INSTRUMENTS GMBH	SEITINGEN-OBERFLACHT Baden-Wurttemberg, DE
3013602181	Blink Medical LTD	Solihull, GB
8010159	A. SCHWEICKHARDT GMBH & CO. KG	Seitingen-Oberflacht Baden-Wurttemberg, DE
1045379	STEPHENS INSTRUMENTS, INC	LEXINGTON, KY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010553238. Last updated year: 2026. Please use registration number 3010553238 when referencing this establishment in official correspondence.