FDA device listing

PrimePad - 1,PrimePad-1-21,PrimePad- 1S,PrimePad-1s-21,PrimePad - 2,PrimePad - 2S,PrimePad - 3,PrimePad - 3S,PrimePad…

FDA device listing 1932540797 · G&T Industries

Key facts

Proprietary names PrimePad - 1,PrimePad-1-21,PrimePad- 1S,PrimePad-1s-21,PrimePad - 2,PrimePad - 2S,PrimePad - 3,PrimePad - 3S,PrimePad - BBO,PrimePad - CVP,PrimePad - K1,PrimePad - K10,PrimePad -K2,PrimePad-K2-21,PrimePad - K3,PrimePad - K4,PrimePad - K5,PrimePad - K6,PrimePad - K7,PrimePad - K8,PrimePad - K9,PrimePad-K9-21,PrimePad…
Owner/operator G&T Industries
Owner/operator number 10038701
Product codes LWG
Device names LWG - Surgical Table Cushion
Device class Class I
Classification regulations (21 CFR) 878.4950
Review panels General & Plastic Surgery
Registered establishments G&T Industries Reading, PA Facility
Establishment registrations 3011389136
FEI numbers 3011389136
Establishment operations Contract Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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