PLAYHOUSE METHOD INC. D/B/A PLAYHOUSE MD

FDA Device Registration & Listing · Santa Monica, CA, US · Registration 3038282348

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
3038282348
FEI Number
3038282348
Entity Name
PLAYHOUSE METHOD INC. D/B/A PLAYHOUSE MD
City/State/Country
Santa Monica, CA, US
Establishment Address
2450 Colorado Ave Ste 100e, Santa Monica, CA 90404, US
Establishment Type(s)
Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Playhouse Method Inc. d/b/a Playhouse MD (Owner Number: 10093460)
Owner / Operator Contact Address
2450 Colorado Avenue, Ste 100E, Santa Monica, CA 90404, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Playhouse MD Fever Buddy 3-in-1 Infrared Thermometer - Giraffe (#1051) Playhouse MD Fever Buddy 3-in-1 Infrared Thermometer - Giraffe (#1051-R) Playhouse MD Medicine Buddy Medicine Dispenser - Rocket (#1011) Playhouse MD Medicine Buddy Medicine Dispenser - Butter­fly (#1012) Playhouse MD Booger Buddy Light-Up Nasal Aspirator - Elephant (#1021) Playhouse MD Booger Buddy Light-Up Nasal Bulb - Narwhal (#1031)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SDV Clinical Electronic Thermometer General Hospital Class 2 880.2910 2025-12-15
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2025-05-19
BSY Catheters, Suction, Tracheobronchial Anesthesiology Class 1 868.6810 2025-05-19

Official Correspondent

Michael Kamins

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Playhouse Method Inc. d/b/a Playhouse MD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038282348. Last updated year: 2026. Please use registration number 3038282348 when referencing this establishment in official correspondence.
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