Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3035371880

FEI Number

3035371880

Entity Name

BEBIRD USA, INC.

City/State/Country

Redondo Beach, CA, US

Establishment Address

2613 Manhattan Beach Blvd, Redondo Beach, CA 90278, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Bebird USA, Inc. (Owner Number: 10092537)

Owner / Operator Contact Address

2613 Manhattan Beach Blvd, Redondo Beach, CA 90278, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bebird bebird, Cleaneze

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2025-05-02
JYT	Pick, Microsurgical Ear	Ear, Nose, Throat	Class 1	874.4420	2025-01-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bebird USA, 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
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

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3030089857	Nordes Sp. z o.o.	Wroclaw Dolnoslaskie, PL
9614434	STORZ ENDOSKOP PRODUKTIONS GMBH	SCHAFFHAUSEN, CH

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035371880. Last updated year: 2026. Please use registration number 3035371880 when referencing this establishment in official correspondence.