OBBOMED GROUP LLC

FDA Device Registration & Listing · Pomona, CA, US · Registration 3011447447

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
3011447447
FEI Number
3011447447
Entity Name
OBBOMED GROUP LLC
City/State/Country
Pomona, CA, US
Establishment Address
1210 E Lexington Ave, Pomona, CA 91766, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Obbomed Group LLC (Owner Number: 10048805)
Owner / Operator Contact Address
1210 E Lexington Ave, Pomona, CA 91766, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Disposable Medical Protective Clothing Disposable Non-Surgical Isolation Gown Goggle Face Shield ObboMed Group LLC 3 Layer Disposable Mask KN95 Protective Mask 3 Layer Disposable Mask (Children's Mask)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OEA Non-Surgical Gown General, Plastic Surgery Class 1 878.4040 2020-08-07
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2020-08-07
FNM Mattress, Air Flotation, Alternating Pressure General Hospital Class 2 880.5550 2019-12-10
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2020-04-06

Official Correspondent

Allen Liang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Obbomed Group LLC
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
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011447447. Last updated year: 2026. Please use registration number 3011447447 when referencing this establishment in official correspondence.
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