Salaera d.b.a Perma Pure

FDA Device Registration & Listing · Lakewood, NJ, US · Registration 2244684

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
2244684
FEI Number
2244684
Entity Name
Salaera d.b.a Perma Pure
City/State/Country
Lakewood, NJ, US
Establishment Address
1001 New Hampshire Avenue, Unit B, Lakewood, NJ 08701, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Salaera, LLC d.b.a Perma Pure (Owner Number: 2244684)
Owner / Operator Contact Address
1001 New Hampshire Avenue, Unit B, Lakewood, NJ 08701, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CBQ Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration) Anesthesiology Class 2 868.1500 2013-11-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Salaera, LLC d.b.a Perma Pure
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
K040917 Philips Medizin Systeme Boeblingen GmbH PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B 2004-04-29

Similar Registrations

Registration Number Establishment Name Location
3009156722 SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. Shenzhen Guangdong, CN
3019388613 Masimo Corporation Irvine, CA, US
3004415070 KB Components Finland Oy Nurmijarvi Etela-Karjala, FI
3007305624 GUANGDONG BIOLIGHT MEDITECH CO., LTD Zhuhai Guangdong, CN
3009831876 MASIMO CORPORATION Irvine, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2244684. Last updated year: 2026. Please use registration number 2244684 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.