Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015238043

FEI Number

3015238043

Entity Name

RECIBIO, INC.

City/State/Country

Richmond, TX, US

Establishment Address

1803 Rock Fence, Richmond, TX 77406, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Recibio, Inc. (Owner Number: 10059285)

Owner / Operator Contact Address

1860 FM 359 #171, Richmond, TX 77406, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CeaLogic - Ratio Applicator Kit Cealogic Film CeaLogic Specimen Collection Kit CeaLogic Amniotic Perforator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2020-03-23
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2026-01-11
BYZ	Trap, Sterile Specimen	General Hospital	Class 2	880.6740	2018-12-18
HGE	Amniotome	Obstetrics/Gynecology	Class 1	884.4530	2018-12-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Recibio, 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
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

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3044994756	SUNMED AP, LTD., WAREHOUSE NO. 2	ZHUHAI Guangdong, CN
2084346	MARINA MEDICAL INSTRUMENTS, INC.	Davie, FL, US
1416980	BAXTER HEALTHCARE CORPORATION	ROUND LAKE, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015238043. Last updated year: 2026. Please use registration number 3015238043 when referencing this establishment in official correspondence.