Berchtold Corp.
Berchtold Corp. holds FDA 510(k) medical device clearance, cleared in 2002, with 5 FDA device recalls on record.
Top product codes for Berchtold Corp.
FDA recalls by Berchtold Corp.
- Z-1925-2016 — Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional accessory to the Operon Surgical Table. The pads may be attached to the base section with a Velcro fastener. The HybriGel pad shapes and variants can differ depending on the scope of the delivery.
- Z-0154-2016 — TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a ceiling mounted device to supply power, medical gases, and data-communication services. TELETOM is designed to be used in rooms that have been constructed to meet National Fire Protection Association.
- Z-1488-2013 — Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables
- Z-2148-2012 — Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual recording of surgical procedures.
- Z-2168-2013 — OPERON D850 Surgical Table Product Usage: Surgical Table
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Berchtold Corp.
Data sourced from openFDA. This site is unofficial and independent of the FDA.