STILLE SURGICAL INC.

FDA Device Registration & Listing · Lombard, IL, US · Registration 1648279

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
1648279
FEI Number
1000516389
Entity Name
STILLE SURGICAL INC.
City/State/Country
Lombard, IL, US
Establishment Address
840 Parkview Blvd, Lombard, IL 60148, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
STILLE SURGICAL INC. (Owner Number: 9012232)
Owner / Operator Contact Address
840 Parkview Blvd., --, Lombard, IL 60148, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
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
GDC Table, Operating-Room, Electrical General, Plastic Surgery Class 1 878.4960 2024-01-31
LGX Table, Examination, Medical, Powered General, Plastic Surgery Class 1 878.4960 2021-08-24

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

STILLE SURGICAL INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1648279. Last updated year: 2026. Please use registration number 1648279 when referencing this establishment in official correspondence.
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