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Synergetics Inc

Company MO
Found in 4 federal databases · 30 total records
co_sos 1 records
CO Business: SYNERGETICS INCORPORATED 1995-03-13
DPC | Status: Good Standing | Fort Collins, CO
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epa_echo 1 records
EPA ECHO: Synergetics 2009-09-30
Type: Administrative - Formal
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fda 27 records
FDA Device Recall: BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravit 2024-07-17
Class I — Sterilization certificates could not be validated by the supplier
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FDA Device Recall: BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration 2024-07-17
Class I — Sterilization certificates could not be validated by the supplier
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FDA Device Recall: BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the admin 2024-07-17
Class I — Sterilization certificates could not be validated by the supplier
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FDA Recall: Synergetics Inc — Class II 20161026
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification. | Product: 25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E,...
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FDA Device Recall: 25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E 2016-10-26
Class II — Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
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FDA Device Recall: 25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator, Product 2016-10-26
Class II — Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
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FDA Recall: Synergetics Inc — Class II 20140205
Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure. | Product: 23ga Chow Illuminated Pick, Synergetics, inc., length 7.5 f...
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FDA Recall: Synergetics Inc — Class II 20140205
Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure. | Product: 25ga Endo Illuminator, Synergetics, inc., length 7.0 ft, st...
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FDA Recall: Synergetics Inc — Class II 20140205
Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure. | Product: 23ga Mid-Field Endo Illuminator, Synergetics length 7.5 ft,...
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FDA Device Recall: 23ga Chow Illuminated Pick, Synergetics, inc., length 7.5 ft, sterile / EO, 56.0 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 25ga Endo Illuminator, Synergetics, inc., length 7.0 ft, sterile / EO, 56.02.25 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 23ga Mid-Field Endo Illuminator, Synergetics length 7.5 ft, sterile / EO, 56.22. 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 23ga Chandelier Infusion Cannula, Synergetics, inc., length 8.0 ft, sterile / EO 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: Stiff 25ga Wide Field Endo Illuminator, Synergetics, inc. length 7.5 ft, sterile 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 27ga ONE-STEP (tm) Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: Chandelier Infusion Cannula, Synergetics, inc., 20ga, length 7.5 ft, sterile / E 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 25ga Awh Vivid Chandelier, Synergetics, length 7.5 ft, sterile / EO, 56.54.25P. 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 23ga Aspirating Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.2 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 23ga Straight Fixed Extended Illuminated Laser Probe, Synergetics, length 7.5 ft 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: Two-Port Vitrectomy (TPV (tm)) Wide Field High Flow End Irrigator, Synergetics, 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: Stiff 25ga Chow Illuminated Pick (Dull), Synergetics, inc., length 8.0 ft, ster 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 25ga Aspirating Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.2 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: Endo Illuminator, Synergetics, inc., 20ga, length 7.0 ft, sterile / EO, 56.02. P 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: "The Corona" Shielded Wide Field Endo Illuminator, Synergetics, inc. 20ga, lengt 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 25ga Awh Chandelier, Synergetics, inc., length 8.0 ft, sterile / EO, 56.50.25P. 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: 25ga Mid-Field Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.22 2014-02-05
Class II — Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
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FDA Device Recall: Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog numb 2013-10-30
Class II — One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23 gauge cannulas; the product is labeled as 25 gauge cannulas.
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ny_corps 1 records
NY Corp: SYNERGETICS, INC. 2007-02-21
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Missouri
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