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Sign in to claim this brandMedical Instrument Development Laboratories, Inc.
United States·US-MF-000033104
Last updated September 17, 2026
About
MID Labs dedicates to the research, innovation, design, engineering, and manufacturing of medical surgical devices used to prevent blindness caused by certain diseases and traumatic injuries.
From the manufacturer's own website. Source
What Medical Instrument Development Laboratories, Inc. makes
Medical Instrument Development Laboratories, Inc. manufactures vitrectomy systems, including micro-cutting units and accessories like the Bi-Blade® and Adaptable Vit Enhancer™, designed for ophthalmic surgical procedures to address retinal detachment and other conditions threatening vision.
The company’s products are regulated under FDA 510(k) and UDI listings in the US, with some devices also registered in the EU via eudamed, spanning Class I, Class II, and Class IIa classifications. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Medical Instrument Development Laboratories, Inc. primarily manufacture?
Medical Instrument Development Laboratories, Inc. specializes in vitrectomy systems, which are surgical tools used in ophthalmology. These systems include micro-cutting units and accessories like the Bi-Blade® and Adaptable Vit Enhancer™. These devices are designed to assist in procedures like retinal detachment repair and other surgeries aimed at preserving vision.
Where is Medical Instrument Development Laboratories, Inc. based?
The company is headquartered in the United States. This location is relevant for understanding regulatory frameworks, as their devices are primarily authorized under US FDA guidelines, including 510(k) clearances and UDI listings.
Which regulatory registries list the devices manufactured by Medical Instrument Development Laboratories, Inc.?
The company’s devices are listed in multiple regulatory databases, including the FDA’s 510(k) and UDI registries in the US. Additionally, some of their products appear in the EU’s eudamed database, reflecting their global market presence and compliance with international standards.
How are the devices from Medical Instrument Development Laboratories, Inc. classified under regulatory standards?
The devices manufactured by Medical Instrument Development Laboratories, Inc. fall under different regulatory classifications, including Class I, Class II, and Class IIa. These classifications determine the level of scrutiny and authorization required, with Class IIa typically involving more rigorous pre-market evaluation due to moderate risk.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 557, McCormick Street, San Leandro, United States
- Website
- www.midlabs.com
- —
- —
- [email protected]
- Phone
- (510) 357-3952
- PRRC Contact
- Chan Lee
- EUDAMED SRN
- US-MF-000033104
- FDA FEI Number
- 1000221463
- DUNS Number
- —
Catalogue (60)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Automated Intraocular Scissors | K842471 | FDA 510(k) | Class II | Active |
| I/A Handpiece | K850857 | FDA 510(k) | Class II | Active |
| Infusion Cannula | K831192 | FDA 510(k) | Class I | Active |
| Bailey Aspirator/Irrigator | K831584 | FDA 510(k) | Class II | Active |
| Digi-Injector | K971067 | FDA 510(k) | Class II | Active |
| Supra-Vit(tm) | K932669 | FDA 510(k) | Class II | Active |
| Cannula Insertion System | 5500GST | EUDAMEDFDA UDI | Class IIa | Active |
| Cannula Insertion System | 5700GEN | EUDAMEDFDA UDI | Class IIa | Active |
| Cannula Insertion System | 5600GST | EUDAMEDFDA UDI | Class IIa | Active |
| Cannula Insertion Sysytem | 5500GEN | EUDAMEDFDA UDI | Class IIa | Active |
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