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Micro Surgery Handpiece SGS, Model: SGS-E2S, Order Code: H266, Manufactured by: Nakanishi Inc The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible..

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Surgical Handpiece, Model: SGA-E Order Code: H083, Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Micro Surgery Handpiece SGS, Model: SGS-ES, Order Code: H264, Manufactured by: Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Surgical Handpiece, Model: SGS-E, Order Code: H084, Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Surgical Handpiece, Model: SGS-E2G Order Code: H185, Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Micro Surgery Handpiece SGA, Model SGA-ES, Order Code:H263, Manufactured by: Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Surgical Handpiece, Model: SGA-E2G Order Code: H184, Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Micro Surgery Handpiece SGA, Model SGA-E2S Order Code: H265, Manufactured by: Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code KMW·June 1, 2018

Diamond Coated Tips and Burs are accessories to the air powered dental handpiece (S-MAX pico) The intended use of the tips is based on the parent device. For burs used with the dental handpieces, the intended use is general dental actions such as removing carious material, reducing hard tooth structure, cavity preparation, finishing tooth preparations and restorations and polishing teeth.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code EFB·July 8, 2016

Diamond Coated Tips and Burs are accessories to the air powered Bone drill (VARIOSURG with and without light) The intended use of the tips is based on the parent device. For the VarioSurg, in addition to the scaling functions, diamond coated tips are used for socket lift, sinus lift, and implant preparation.

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code ELC·July 8, 2016

Diamond Coated Tips and Burs are accessories to the Ultrasonic Scaler (VARIOS 350 LUX, VARIOS 350, VARIOS 150 LUX, VARIOS 150). The intended use of the tips is based on the parent device. For the ultrasonic scalers and the sonic air scaler, the tips are used for various actions such as scaling (removal of calculus), periodontics (root planing and maintenance), endodontics (root canal enlarging, irrigation, and filling), restorative (caries removal and tooth surface detailing).

FDA Recall
Terminated ·Nakanishi Inc. 700 Shimohinata Kanuma Japan·Product code ELC·July 8, 2016

Breathe Right Clear, 30 ct. carton., UPC 7-57145-00246-7 (US), UPC 9-300673-871749 (AU/NZ)

FDA Recall
Terminated ·GSK Consumer Healthcare·Product code N/A·April 25, 2016

Breathe Right Clear, 30 ct. carton., UPC 7-57145-00246-7 (US), UPC 9-300673-871749 (AU/NZ)

FDA Enforcement
Class III ·Terminated·GSK Consumer Healthcare·July 20, 2016

Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-PCAM1, g) ASK-45703-PCCH2, h) ASK-45703-PN; catheter introducer

FDA Recall
Terminated ·ARROW INTERNATIONAL Inc.·Product code FOZ·October 27, 2022

ACCESS TRAY/Product SKU's (Codes) ASK-03000-CHUQ, ASK-03000-CHUQ1, ASK-04001-GFH, ASK-04001-SUH and ASK-04001-UHC. Access tray for epidural anesthesia kit

FDA Recall
Terminated ·Arrow International Inc·Product code CAZ·October 29, 2010

Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Codes: ASK-42703-PAM1, ASK-42703-PSHR1, ASK-45703-PNY, ASK-45703-PWHC1

FDA Recall
Terminated ·Arrow International Inc·Product code FOZ·April 11, 2018

Radial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1

FDA Recall
Terminated ·Arrow International Inc·Product code DQX·April 11, 2018

Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-PCAM1, g) ASK-45703-PCCH2, h) ASK-45703-PN; catheter introducer

FDA Enforcement
Class I ·Terminated·ARROW INTERNATIONAL Inc.·December 21, 2022

Arrow 4FR Peripherally Inserted Central Catheter (PICCs) Kits. Product numbers: ASK-01451-BMH; ASK-05041-CHC; ASK-05041-CHC1; ASK-05041-CHM; ASK-05041-HMC; ASK-05041-QV; ASK-07041-BMH; CN-05041-LW; MSO-01451-UCL; MTO-01451-RH; PL-05041; PR-04041-HPX; PR-05041; PR-05041-HP; PR- 05041-HPX; PR-05041-LW; PR-05041-MW; PR-05041-T; PR-05042; PR-05541-HPX; PR-07041-PTSP; and RJ-01451-W.

FDA Recall
Terminated ·Arrow International Inc·Product code LJS·March 29, 2010

Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes

FDA Enforcement
Class II ·Terminated·Arrow International Inc·October 7, 2015