R.H. CROSS ENTERPRISES, INC.

FDA Device Registration & Listing · Portage, MI, US · Registration 3010141593

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
3010141593
FEI Number
3010141593
Entity Name
R.H. CROSS ENTERPRISES, INC.
City/State/Country
Portage, MI, US
Establishment Address
6080 Corporate Ave, Portage, MI 49002, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
R.H. CROSS ENTERPRISES, INC. (Owner Number: 10043320)
Owner / Operator Contact Address
6080 Corporate Ave, Portage, MI 49002, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Triton AI Calibration Placard Stryker® LIGHT MINERAL OIL / Non-Sterile Stryker® TPS STANDARD ATTACHMENT BRUSH Stryker® TPS Micro Drill / Elite Attachment Brush Triton 2L Canister Insert Kit Triton 3L Canister Insert Kit Stryker® Wire Holder

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PBZ Image Processing Device For Estimation Of External Blood Loss General Hospital Class 2 880.2750 2025-06-30
DWG Electrosurgical Device General, Plastic Surgery Class 2 878.4400 2013-02-05
GET Motor, Surgical Instrument, Pneumatic Powered General, Plastic Surgery Class 1 878.4820 2013-02-05
EIA Unit, Operative Dental Dental Class 1 872.6640 2021-02-23
PBZ Image Processing Device For Estimation Of External Blood Loss General Hospital Class 2 880.2750 2025-06-30
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2013-02-05

Official Correspondent

TRAVIS MANN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

R.H. CROSS ENTERPRISES, INC.
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
K953432 Midas Rex Pneumatic Tools, Inc. ROTATING, FIXED FOOTED, FIXED SHIELD ATTACHMENTS, DISSECTING TOOLS 1995-09-14

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0332-2022 Covidien Llc U
Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information on the battery charging progress and battery pack status Item Code: CBCA

Similar Registrations

Registration Number Establishment Name Location
3015967359 Stryker Instruments Portage, MI, US
3031240334 MEDCARE SOLUTIONS GMBH Emmingen Baden-Wurttemberg, DE
1057358 RG Medical USA Mount Juliet, TN, US
3007305485 Consolidated Medical Equipment Company Chihuahua, MX
1320894 CONMED CORPORATION Utica, NY, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010141593. Last updated year: 2026. Please use registration number 3010141593 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.