PERIDOT CORPORATION

FDA Device Registration & Listing · Pleasanton, CA, US · Registration 3007503337

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
3007503337
FEI Number
3007503337
Entity Name
PERIDOT CORPORATION
City/State/Country
Pleasanton, CA, US
Establishment Address
1072 Serpentine Lane, Pleasanton, CA 94566, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Peridot Corporation (Owner Number: 10050501)
Owner / Operator Contact Address
1072 Serpentine Lane, Pleasanton, CA 94566, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JDR Staple, Fixation, Bone Orthopedic Class 2 888.3030 2015-11-24

Official Correspondent

Ron LeTendre

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Peridot Corporation
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
K153770 In2bones Sas OS2(R)-VP Varisation Staple 2016-03-21

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2023 Synthes (USA) Products LLC 2
Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001

Similar Registrations

Registration Number Establishment Name Location
3039081660 BLAZE BIOTECH, LLC San Antonio, TX, US
3027848094 MENTOR SUPPLY CHAIN (USA) INC Warsaw, IN, US
3014527966 F & A FOUNDATION Tulsa, OK, US
1833920 INSTRU-MED TECHNOLOGIES Warsaw, IN, US
1058584 Sterigenics US LLC Charlotte, NC, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007503337. Last updated year: 2026. Please use registration number 3007503337 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.